GENERAL PROTECTION
avobenzone,octinoxate,octisalate,octocrylene gel |
Product Information |
Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 71153-2012 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) | OCTISALATE | 3 g in 1 mL |
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) | OCTINOXATE | 7.5 g in 1 mL |
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) | AVOBENZONE | 3 g in 1 mL |
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) | OCTOCRYLENE | 2 g in 1 mL |
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Inactive Ingredients |
Ingredient Name | Strength |
XANTHAN GUM (UNII: TTV12P4NEE) | |
ALOE VERA LEAF (UNII: ZY81Z83H0X) | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 71153-2012-1 | 44 mL in 1 TUBE; Type 0: Not a Combination Product | 02/01/2017 | |
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Marketing Information |
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
OTC monograph final | part352 | 02/01/2017 | |
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