- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
- For sunscreen use:
- apply liberally 15 minutes before sun exposure
- children under 6 months of age: ask a doctor
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
Other Information
- protect the product in this container from excessive heat and direct sun
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INACTIVE INGREDIENT
Inactive Ingredients/Ingrédients inactifs: WATER/EAU, DIMETHICONE, BUTYLENE GLYCOL, SILICA, GLYCERIN, ETHYLHEXYL PALMITATE, PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE, STEARETH-21, SORBITAN STEARATE, BORON NITRIDE, MAGNESIUM ALUMINUM SILICATE, TRIETHANOLAMINE, METHYLPARABEN, GLYCERYL STEARATE, STEARETH-2, SODIUM HEXAMETAPHOSPHATE, XANTHAN GUM, BHT, DISODIUM EDTA, FRAGRANCE/PARFUM. MAY CONTAIN/PEUT CONTENIR: IRON OXIDES, TITANIUM DIOXIDE/CI 77891, FERRIC AMMONIUM FERROCYANIDE/CI 77510.
- QUESTIONS
- PACKAGE LABEL
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INGREDIENTS AND APPEARANCE
TRUE COLOR IDEAL NUDE MATTE FOUNDATION SPF20
true color ideal nude matte foundation spf20 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-9504 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-9504-2 1 in 1 CARTON 01/01/2017 1 NDC:10096-9504-1 30 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 01/01/2017 Labeler - New Avon LLC (080143520)