| Product NDC: | 10056-646 |
| Proprietary Name: | Artistry Ideal Dual Foundation |
| Non Proprietary Name: | OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 6; 2.7 g/100g; g/100g & nbsp; OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10056-646 |
| Labeler Name: | Access Business Group LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110414 |
| Package NDC: | 10056-646-12 |
| Package Description: | 1 CONTAINER in 1 BOX (10056-646-12) > 12 g in 1 CONTAINER |
| NDC Code | 10056-646-12 |
| Proprietary Name | Artistry Ideal Dual Foundation |
| Package Description | 1 CONTAINER in 1 BOX (10056-646-12) > 12 g in 1 CONTAINER |
| Product NDC | 10056-646 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110414 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Access Business Group LLC |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 6; 2.7 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |