| Product NDC: | 64127-084 |
| Proprietary Name: | G.M. Collin Mineral Sun Veil |
| Non Proprietary Name: | zinc oxide |
| Active Ingredient(s): | .125 mL/mL & nbsp; zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64127-084 |
| Labeler Name: | Laboratoires Dermo Cosmetik Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100517 |
| Package NDC: | 64127-084-01 |
| Package Description: | 1 TUBE in 1 KIT (64127-084-01) > 50 mL in 1 TUBE |
| NDC Code | 64127-084-01 |
| Proprietary Name | G.M. Collin Mineral Sun Veil |
| Package Description | 1 TUBE in 1 KIT (64127-084-01) > 50 mL in 1 TUBE |
| Product NDC | 64127-084 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100517 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Dermo Cosmetik Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | .125 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |