Product NDC: | 41250-820 |
Proprietary Name: | Moisturizer |
Non Proprietary Name: | octinoxate, octisalate, oxybenzone |
Active Ingredient(s): | 8.86; 5.9; 3.54 mL/118mL; mL/118mL; mL/118mL & nbsp; octinoxate, octisalate, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41250-820 |
Labeler Name: | Meijer Distribution Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090504 |
Package NDC: | 41250-820-26 |
Package Description: | 1 BOTTLE in 1 CARTON (41250-820-26) > 118 mL in 1 BOTTLE |
NDC Code | 41250-820-26 |
Proprietary Name | Moisturizer |
Package Description | 1 BOTTLE in 1 CARTON (41250-820-26) > 118 mL in 1 BOTTLE |
Product NDC | 41250-820 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octinoxate, octisalate, oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090504 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Meijer Distribution Inc |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 8.86; 5.9; 3.54 |
Strength Unit | mL/118mL; mL/118mL; mL/118mL |
Pharmaceutical Classes |