Product NDC: | 10096-0103 |
Proprietary Name: | moisture therapy |
Non Proprietary Name: | Octinoxate, Oxybenzone |
Active Ingredient(s): | 1.125; .45 mL/15mL; mL/15mL & nbsp; Octinoxate, Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0103 |
Labeler Name: | Avon Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120522 |
Package NDC: | 10096-0103-1 |
Package Description: | 15 mL in 1 TUBE, WITH APPLICATOR (10096-0103-1) |
NDC Code | 10096-0103-1 |
Proprietary Name | moisture therapy |
Package Description | 15 mL in 1 TUBE, WITH APPLICATOR (10096-0103-1) |
Product NDC | 10096-0103 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Oxybenzone |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20120522 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc. |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 1.125; .45 |
Strength Unit | mL/15mL; mL/15mL |
Pharmaceutical Classes |