Product NDC: | 46007-202 |
Proprietary Name: | AGE DEFYING MOISTURIZER |
Non Proprietary Name: | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
Active Ingredient(s): | 2; 7.5; 5; 6 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 46007-202 |
Labeler Name: | Skin Authority LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120419 |
Package NDC: | 46007-202-12 |
Package Description: | 50 mL in 1 BOTTLE (46007-202-12) |
NDC Code | 46007-202-12 |
Proprietary Name | AGE DEFYING MOISTURIZER |
Package Description | 50 mL in 1 BOTTLE (46007-202-12) |
Product NDC | 46007-202 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120419 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Skin Authority LLC |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 2; 7.5; 5; 6 |
Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes |