| Product NDC: | 62499-420 |
| Proprietary Name: | SPF 15 Protective Balm with UVA/UVB Sunscreens |
| Non Proprietary Name: | Octinoxate Octisalate Oxybenzone |
| Active Ingredient(s): | 7.5; 3; 3 g/100g; g/100g; g/100g & nbsp; Octinoxate Octisalate Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62499-420 |
| Labeler Name: | Laboratoire Dr Renaud inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110321 |
| Package NDC: | 62499-420-11 |
| Package Description: | 1 CARTRIDGE in 1 BOX (62499-420-11) > 3.8 g in 1 CARTRIDGE (62499-420-02) |
| NDC Code | 62499-420-11 |
| Proprietary Name | SPF 15 Protective Balm with UVA/UVB Sunscreens |
| Package Description | 1 CARTRIDGE in 1 BOX (62499-420-11) > 3.8 g in 1 CARTRIDGE (62499-420-02) |
| Product NDC | 62499-420 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Octisalate Oxybenzone |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110321 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Laboratoire Dr Renaud inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 3; 3 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |