Product NDC: | 10096-0301 |
Proprietary Name: | Avon Elements |
Non Proprietary Name: | Octinoxate, Octisalate, Avobenzone |
Active Ingredient(s): | 28.5; 75; 47.5 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0301 |
Labeler Name: | Avon Products, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130401 |
Package NDC: | 10096-0301-2 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (10096-0301-2) > 118 mL in 1 BOTTLE, PUMP (10096-0301-1) |
NDC Code | 10096-0301-2 |
Proprietary Name | Avon Elements |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (10096-0301-2) > 118 mL in 1 BOTTLE, PUMP (10096-0301-1) |
Product NDC | 10096-0301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, Avobenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | 28.5; 75; 47.5 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |