| Product NDC: | 62499-445 |
| Proprietary Name: | SPF 15 Anti-shine moisturizing |
| Non Proprietary Name: | OCTINOXATE and OCTOCRYLENE |
| Active Ingredient(s): | 7.77; .1 g/100g; g/100g & nbsp; OCTINOXATE and OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62499-445 |
| Labeler Name: | Laboratoire Dr Renaud Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111129 |
| Package NDC: | 62499-445-11 |
| Package Description: | 1 TUBE in 1 CARTON (62499-445-11) > 50 g in 1 TUBE (62499-445-04) |
| NDC Code | 62499-445-11 |
| Proprietary Name | SPF 15 Anti-shine moisturizing |
| Package Description | 1 TUBE in 1 CARTON (62499-445-11) > 50 g in 1 TUBE (62499-445-04) |
| Product NDC | 62499-445 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OCTOCRYLENE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111129 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoire Dr Renaud Inc. |
| Substance Name | OCTINOXATE; OCTOCRYLENE |
| Strength Number | 7.77; .1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |