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) |
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 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 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 | |
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