Product NDC: | 11701-050 |
Proprietary Name: | Critic Aid Skin |
Non Proprietary Name: | Petrolatum and Zinc oxide |
Active Ingredient(s): | 510; 200 mg/g; mg/g & nbsp; Petrolatum and Zinc oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11701-050 |
Labeler Name: | Coloplast Manufacturing US, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090615 |
Package NDC: | 11701-050-32 |
Package Description: | 170 g in 1 TUBE (11701-050-32) |
NDC Code | 11701-050-32 |
Proprietary Name | Critic Aid Skin |
Package Description | 170 g in 1 TUBE (11701-050-32) |
Product NDC | 11701-050 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Petrolatum and Zinc oxide |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20090615 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Coloplast Manufacturing US, LLC |
Substance Name | PETROLATUM; ZINC OXIDE |
Strength Number | 510; 200 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |