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Moisture Renew
Moisture Renew - 76485-1022-1 - (Octinoxate)
Drug Information of Moisture Renew
| Product NDC: | 76485-1022 |
| Proprietary Name: | Moisture Renew |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 300; 80 mg/4g; mg/4g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Moisture Renew
| Product NDC: | 76485-1022 |
| Labeler Name: | Rimmel Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111020 |
Package Information of Moisture Renew
| Package NDC: | 76485-1022-1 |
| Package Description: | 4 g in 1 TUBE (76485-1022-1) |
NDC Information of Moisture Renew
| NDC Code | 76485-1022-1 |
| Proprietary Name | Moisture Renew |
| Package Description | 4 g in 1 TUBE (76485-1022-1) |
| Product NDC | 76485-1022 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20111020 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rimmel Inc. |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | 300; 80 |
| Strength Unit | mg/4g; mg/4g |
| Pharmaceutical Classes |
