Product NDC: | 10096-0188 |
Proprietary Name: | Ultra Color Rich |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
Active Ingredient(s): | 150; 90 mg/3g; mg/3g & nbsp; OCTINOXATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0188 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091222 |
Package NDC: | 10096-0188-1 |
Package Description: | 3 g in 1 CASE (10096-0188-1) |
NDC Code | 10096-0188-1 |
Proprietary Name | Ultra Color Rich |
Package Description | 3 g in 1 CASE (10096-0188-1) |
Product NDC | 10096-0188 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20091222 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 150; 90 |
Strength Unit | mg/3g; mg/3g |
Pharmaceutical Classes |