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Skin Activator Day
Skin Activator Day - 51785-086-20 - (Octinoxate, Octisalate and Avobenzone)
Drug Information of Skin Activator Day
| Product NDC: | 51785-086 |
| Proprietary Name: | Skin Activator Day |
| Non Proprietary Name: | Octinoxate, Octisalate and Avobenzone |
| Active Ingredient(s): | .0198; .0742; .0495 g/mL; g/mL; g/mL & nbsp; Octinoxate, Octisalate and Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Skin Activator Day
| Product NDC: | 51785-086 |
| Labeler Name: | Herbalife International of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111021 |
Package Information of Skin Activator Day
| Package NDC: | 51785-086-20 |
| Package Description: | 1 TUBE in 1 CARTON (51785-086-20) > 50 mL in 1 TUBE |
NDC Information of Skin Activator Day
| NDC Code | 51785-086-20 |
| Proprietary Name | Skin Activator Day |
| Package Description | 1 TUBE in 1 CARTON (51785-086-20) > 50 mL in 1 TUBE |
| Product NDC | 51785-086 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate and Avobenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111021 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Herbalife International of America, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | .0198; .0742; .0495 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |
