Schmid & Son Packaging
NDC Database

Schmid & Son Packaging

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Human OTC Drug
  • Total Records 26
  • Latest Marketing Date 2026-01-01
  • Data Source FDA
  • First Marketing Date 2022-08-01
Company Overview

Company

Schmid & Son Packaging

Country

U.S.A

Social Profiles

Company Snapshot

Schmid & Son Packaging

7699 95th St S #3945, Cottage Grove, MN 55016

U.S.A

www.schmidpackaging.com/ steve@schmidpackaging.com View on Map
NDC Records ( 26 records )
2022
01 Aug
Human OTC Drug NDC: 51630-114

Nonproprietary Name

Hand Sanitizer

Dosage Form

LIQUID

Strength

0.12 mg/mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-114

Substance

BENZALKONIUM CHLORIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2022-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Oct
Human OTC Drug NDC: 51630-116

Nonproprietary Name

Coola Refreshing Water Face Cream

Dosage Form

CREAM

Strength

3; 5; 3; 5 g/100mL; g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-116

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2022-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Nov
Human OTC Drug NDC: 51630-118

Nonproprietary Name

Coola Classic Sunscreen SPF 30 Pina Colada Scent

Dosage Form

SPRAY

Strength

2.8; 4.9; 7.6 g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-118

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2022-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Nov
Human OTC Drug NDC: 51630-119

Nonproprietary Name

Coola Classic Sunscreen SPF 30 Pina Colada 2.0 OZ

Dosage Form

SPRAY

Strength

2.8; 4.9; 7.6 g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-119

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2022-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Mar
Human OTC Drug NDC: 51630-125

Nonproprietary Name

Coola Classic Sunscreen SPF30 Tropical Coconut

Dosage Form

SPRAY

Strength

2.8; 4.9; 7.6 g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-125

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Apr
Human OTC Drug NDC: 51630-126

Nonproprietary Name

Coola Classic Face Lotion Sunscreen 50mL

Dosage Form

LOTION

Strength

17.5; 50; 20; 50 mg/mL; mg/mL; mg/mL; mg/mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-126

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Apr
Human OTC Drug NDC: 51630-127

Nonproprietary Name

Coola Classic Face Mist Sunscreen 50mL

Dosage Form

SPRAY

Strength

2.9; 4.9; 9.5 g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-127

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 May
Human OTC Drug NDC: 51630-128

Nonproprietary Name

Coola Mineral Body Sunscreen SPF 30 Tropical Coconut

Dosage Form

LOTION

Strength

14.2 g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-128

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Jan
Human OTC Drug NDC: 51630-129

Nonproprietary Name

Vacation Arizona Lip Balm

Dosage Form

STICK

Strength

.03; .05; .03; .1 g/g; g/g; g/g; g/g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-129

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
01 Oct
Human OTC Drug NDC: 51630-130

Nonproprietary Name

Zinc Oxide

Dosage Form

STICK

Strength

23.8 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-130

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2023-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Apr
Human OTC Drug NDC: 51630-135

Nonproprietary Name

Coola Classic Face Sunscreen Cucumber SPF30

Dosage Form

LOTION

Strength

1.75; 2.5; 1.5; 3.75 g/100mL; g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-135

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Apr
Human OTC Drug NDC: 51630-136

Nonproprietary Name

Coola Lip Balm Sunscreen

Dosage Form

STICK

Strength

2.9; 4.9; 7.6 g/100g; g/100g; g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-136

Substance

AVOBENZONE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Dec
Human OTC Drug NDC: 51630-138

Nonproprietary Name

Benzocaine

Dosage Form

GEL

Strength

200 mg/g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-138

Substance

BENZOCAINE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Dec
Human OTC Drug NDC: 51630-139

Nonproprietary Name

Benzocaine

Dosage Form

SOLUTION

Strength

200 mg/mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-139

Substance

BENZOCAINE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Nov
Human OTC Drug NDC: 51630-140

Nonproprietary Name

Zinc Oxide

Dosage Form

STICK

Strength

18 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-140

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2024-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-142

Nonproprietary Name

Super Lift SPF Lotion

Dosage Form

SPRAY

Strength

20.8 g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-142

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-143

Nonproprietary Name

Pacifica Future Youth Turnaround

Dosage Form

CREAM

Strength

3; 15; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-143

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-145

Nonproprietary Name

Kroger Sunscreen Stick

Dosage Form

STICK

Strength

21 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-145

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-146

Nonproprietary Name

Coola Frangrance Free Sunscreen Spray 2oz

Dosage Form

SPRAY

Strength

2.9; 4.3; 4.9; 9.5 g/100mL; g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-146

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-147

Nonproprietary Name

Coola Guava Mango Sunscreen

Dosage Form

SPRAY

Strength

2.9; 4; 4.9; 9.5 g/100mL; g/100mL; g/100mL; g/100mL

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-147

Substance

AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jan
Human OTC Drug NDC: 51630-148

Nonproprietary Name

Liplux Lip Balm Skinny Dip

Dosage Form

STICK

Strength

3.6; 3 g/100g; g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-148

Substance

TITANIUM DIOXIDE; ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Aug
Human OTC Drug NDC: 51630-152

Nonproprietary Name

Kinesys Pro Sport Clear Mineral Sunscreen Stick

Dosage Form

STICK

Strength

22 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-152

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2025-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
01 Jan
Human OTC Drug NDC: 51630-153

Nonproprietary Name

Zinc Oxide

Dosage Form

OINTMENT

Strength

12.8 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-153

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Jan
Human OTC Drug NDC: 51630-154

Nonproprietary Name

Zinc Oxide

Dosage Form

OINTMENT

Strength

40 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-154

Substance

ZINC OXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Jan
Human OTC Drug NDC: 51630-155

Nonproprietary Name

Benzoyl Peroxide

Dosage Form

GEL

Strength

10 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-155

Substance

BENZOYL PEROXIDE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Jan
Human OTC Drug NDC: 51630-156

Nonproprietary Name

Dimethicone

Dosage Form

GEL

Strength

1.2 g/100g

Labeler

Schmid & Son Packaging

Marketing Category

DRUG FOR FURTHER PROCESSING

51630-156

Substance

DIMETHICONE

Product Type

HUMAN OTC DRUG

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
26 total
  • Human OTC Drug
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

51630-114

Nonproprietary Name

Hand Sanitizer

Labeler

Schmid & Son Packaging

Dosage Form

LIQUID

FDA NDC Data

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Data maintained from official sources

Structured Database

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Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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