Label: ATTITUDE MINERAL SUNSCREEN VANILLA BLOSSOM- zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 61649-002-15, 61649-002-75 - Packager: Bio Spectra
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 9, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
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Uses
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- Helps prevent sunburn
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- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
- Warnings
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Directions
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- Apply liberally 15 minutes before sun exposure
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- Reapply:
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- At least every 2 hours
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- After 40 minutes of swimming or sweathing
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- Immediately after towel drying
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Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging
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- To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
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- Limit time in the sun, especially from 10am–2pm
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- Wear long-sleeved shirts, pants, hats, and sunglasses
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- Ask a doctor for use on children under 6 months of age.
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Inactive ingredients
Aqua, caprylic/capric triglyceride, cetearyl alcohol, cetearyl glucoside, glyceryl isostearate, glyceryl stearate, C10-18 triglycerides, glycerin, polyhydroxystearic acid, ethylhexylglycerin, caprylyl glycol, xanthan gum, sodium gluconate, geranyl acetate (herbal), vanillin, methyldihydrojasmonate (jasmine).
- Other Information
- PRINCIPAL DISPLAY PANEL - 75 g Tube Carton
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INGREDIENTS AND APPEARANCE
ATTITUDE MINERAL SUNSCREEN VANILLA BLOSSOM
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61649-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM GLUCONATE (UNII: R6Q3791S76) GERANYL ACETATE (UNII: 3W81YG7P9R) VANILLIN (UNII: CHI530446X) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61649-002-75 1 in 1 CARTON 07/01/2014 1 75 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:61649-002-15 1 in 1 CARTON 07/01/2014 2 150 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 07/01/2014 Labeler - Bio Spectra (201137051)