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Wild Rose Daily Moisture Sunscreen - 76041-713-50 - (ZINC OXIDE)

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Drug Information of Wild Rose Daily Moisture Sunscreen

Product NDC: 76041-713
Proprietary Name: Wild Rose Daily Moisture Sunscreen
Non Proprietary Name: ZINC OXIDE
Active Ingredient(s): 19    mL/100mL & nbsp;   ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Wild Rose Daily Moisture Sunscreen

Product NDC: 76041-713
Labeler Name: Neal's Yard (Natural Remedies) Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110610

Package Information of Wild Rose Daily Moisture Sunscreen

Package NDC: 76041-713-50
Package Description: 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE

NDC Information of Wild Rose Daily Moisture Sunscreen

NDC Code 76041-713-50
Proprietary Name Wild Rose Daily Moisture Sunscreen
Package Description 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE
Product NDC 76041-713
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110610
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Neal's Yard (Natural Remedies) Limited
Substance Name ZINC OXIDE
Strength Number 19
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Wild Rose Daily Moisture Sunscreen


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