 
                        | Product NDC: | 76041-713 | 
| Proprietary Name: | Wild Rose Daily Moisture Sunscreen | 
| Non Proprietary Name: | ZINC OXIDE | 
| Active Ingredient(s): | 19 mL/100mL & nbsp; ZINC OXIDE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LOTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 76041-713 | 
| Labeler Name: | Neal's Yard (Natural Remedies) Limited | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20110610 | 
| Package NDC: | 76041-713-50 | 
| Package Description: | 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE | 
| NDC Code | 76041-713-50 | 
| Proprietary Name | Wild Rose Daily Moisture Sunscreen | 
| Package Description | 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE | 
| Product NDC | 76041-713 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | ZINC OXIDE | 
| Dosage Form Name | LOTION | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110610 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Neal's Yard (Natural Remedies) Limited | 
| Substance Name | ZINC OXIDE | 
| Strength Number | 19 | 
| Strength Unit | mL/100mL | 
| Pharmaceutical Classes |