| 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 |