Product NDC: | 65966-009 |
Proprietary Name: | LA MER |
Non Proprietary Name: | ZINC OXIDE, OCTINOXATE |
Active Ingredient(s): | 7.5; 10 mL/100mL; mL/100mL & nbsp; ZINC OXIDE, OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65966-009 |
Labeler Name: | MAX HUBER RESEARCH LAB INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20081001 |
Package NDC: | 65966-009-01 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (65966-009-01) > 40 mL in 1 BOTTLE, PLASTIC (65966-009-02) |
NDC Code | 65966-009-01 |
Proprietary Name | LA MER |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (65966-009-01) > 40 mL in 1 BOTTLE, PLASTIC (65966-009-02) |
Product NDC | 65966-009 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE, OCTINOXATE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20081001 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MAX HUBER RESEARCH LAB INC |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 7.5; 10 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |