Product NDC: | 10096-0304 |
Proprietary Name: | Anew Clinical |
Non Proprietary Name: | Avobenzone, Homosalate, Octinoxate, Octocrylene, Oxybenzone |
Active Ingredient(s): | 28; 95; 75; 25.6; 47.5 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Homosalate, Octinoxate, Octocrylene, Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0304 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130522 |
Package NDC: | 10096-0304-5 |
Package Description: | 1.1 g in 1 PACKET (10096-0304-5) |
NDC Code | 10096-0304-5 |
Proprietary Name | Anew Clinical |
Package Description | 1.1 g in 1 PACKET (10096-0304-5) |
Product NDC | 10096-0304 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octocrylene, Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130522 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 28; 95; 75; 25.6; 47.5 |
Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |