Product NDC: | 67676-301 |
Proprietary Name: | All Natural Sunscreen SPF 40 |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 17.5 g/100g & nbsp; ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67676-301 |
Labeler Name: | Sarati International, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19930101 |
Package NDC: | 67676-301-01 |
Package Description: | 84 g in 1 TUBE (67676-301-01) |
NDC Code | 67676-301-01 |
Proprietary Name | All Natural Sunscreen SPF 40 |
Package Description | 84 g in 1 TUBE (67676-301-01) |
Product NDC | 67676-301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19930101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sarati International, Inc. |
Substance Name | ZINC OXIDE |
Strength Number | 17.5 |
Strength Unit | g/100g |
Pharmaceutical Classes |