Product NDC: | 10096-0181 |
Proprietary Name: | Anew Reversalist |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
Active Ingredient(s): | 28.5; 71.1; 47.5; 40 mg/g; mg/g; mg/g; mg/g & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0181 |
Labeler Name: | Avon Products, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091215 |
Package NDC: | 10096-0181-7 |
Package Description: | 1.1 g in 1 PACKET (10096-0181-7) |
NDC Code | 10096-0181-7 |
Proprietary Name | Anew Reversalist |
Package Description | 1.1 g in 1 PACKET (10096-0181-7) |
Product NDC | 10096-0181 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20091215 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 28.5; 71.1; 47.5; 40 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |