Product NDC: | 67692-081 |
Proprietary Name: | Lumene Vitamin C Pure Radiance Day |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 3; 7.5; 4; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67692-081 |
Labeler Name: | LUMENE OY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101122 |
Package NDC: | 67692-081-00 |
Package Description: | 1 JAR in 1 BOX (67692-081-00) > 50 mL in 1 JAR |
NDC Code | 67692-081-00 |
Proprietary Name | Lumene Vitamin C Pure Radiance Day |
Package Description | 1 JAR in 1 BOX (67692-081-00) > 50 mL in 1 JAR |
Product NDC | 67692-081 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101122 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | LUMENE OY |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 7.5; 4; 5 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |