Product NDC: | 41190-503 |
Proprietary Name: | Complete Beauty |
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: | 41190-503 |
Labeler Name: | Wakefern Food Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130109 |
Package NDC: | 41190-503-26 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (41190-503-26) > 118 mL in 1 BOTTLE, PLASTIC |
NDC Code | 41190-503-26 |
Proprietary Name | Complete Beauty |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (41190-503-26) > 118 mL in 1 BOTTLE, PLASTIC |
Product NDC | 41190-503 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, zinc oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130109 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Wakefern Food Corporation |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 60; 30 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |