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 |