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Aveeno Baby Mommy and Me - 58232-9914-9 - (Zinc Oxide and Dimethicone)

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Drug Information of Aveeno Baby Mommy and Me

Product NDC: 58232-9914
Proprietary Name: Aveeno Baby Mommy and Me
Non Proprietary Name: Zinc Oxide and Dimethicone
Active Ingredient(s):    & nbsp;   Zinc Oxide and Dimethicone
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Aveeno Baby Mommy and Me

Product NDC: 58232-9914
Labeler Name: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130510

Package Information of Aveeno Baby Mommy and Me

Package NDC: 58232-9914-9
Package Description: 1 KIT in 1 PACKAGE, COMBINATION (58232-9914-9) * 236 mL in 1 BOTTLE * 354 mL in 1 BOTTLE * 226 mL in 1 TUBE (58232-0211-1) * 59 mL in 1 BOTTLE * 226 mL in 1 TUBE (58232-0104-2) * 51 g in 1 TUBE (58232-0631-2) * 236 mL in 1 BOTTLE

NDC Information of Aveeno Baby Mommy and Me

NDC Code 58232-9914-9
Proprietary Name Aveeno Baby Mommy and Me
Package Description 1 KIT in 1 PACKAGE, COMBINATION (58232-9914-9) * 236 mL in 1 BOTTLE * 354 mL in 1 BOTTLE * 226 mL in 1 TUBE (58232-0211-1) * 59 mL in 1 BOTTLE * 226 mL in 1 TUBE (58232-0104-2) * 51 g in 1 TUBE (58232-0631-2) * 236 mL in 1 BOTTLE
Product NDC 58232-9914
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc Oxide and Dimethicone
Dosage Form Name KIT
Route Name
Start Marketing Date 20130510
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Aveeno Baby Mommy and Me


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