Product NDC: | 10096-0249 |
Proprietary Name: | Moisture Therapy |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 75; 50; 10 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0249 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110411 |
Package NDC: | 10096-0249-1 |
Package Description: | 400 mL in 1 BOTTLE (10096-0249-1) |
NDC Code | 10096-0249-1 |
Proprietary Name | Moisture Therapy |
Package Description | 400 mL in 1 BOTTLE (10096-0249-1) |
Product NDC | 10096-0249 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110411 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 75; 50; 10 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |