Product NDC: | 36800-339 |
Proprietary Name: | Illuminating Daily Moisturizer |
Non Proprietary Name: | Avobenzone, Octisalate and Octocrylene |
Active Ingredient(s): | 3; 5; 8 mL/100mL; mL/100mL; mL/100mL & nbsp; Avobenzone, Octisalate and Octocrylene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36800-339 |
Labeler Name: | Topco Associates LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120511 |
Package NDC: | 36800-339-19 |
Package Description: | 1 BOTTLE in 1 CARTON (36800-339-19) > 120 mL in 1 BOTTLE |
NDC Code | 36800-339-19 |
Proprietary Name | Illuminating Daily Moisturizer |
Package Description | 1 BOTTLE in 1 CARTON (36800-339-19) > 120 mL in 1 BOTTLE |
Product NDC | 36800-339 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Octisalate and Octocrylene |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120511 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Topco Associates LLC |
Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE |
Strength Number | 3; 5; 8 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |