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 |