Product NDC: | 49035-091 |
Proprietary Name: | All Day Moisturizing |
Non Proprietary Name: | Octinoxate, zinc oxide |
Active Ingredient(s): | 60; 30 mg/mL; mg/mL & nbsp; Octinoxate, zinc oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-091 |
Labeler Name: | Wal-Mart Stores, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060407 |
Package NDC: | 49035-091-30 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49035-091-30) > 177 mL in 1 BOTTLE, PLASTIC |
NDC Code | 49035-091-30 |
Proprietary Name | All Day Moisturizing |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49035-091-30) > 177 mL in 1 BOTTLE, PLASTIC |
Product NDC | 49035-091 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, zinc oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20060407 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Wal-Mart Stores, Inc |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 60; 30 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |