Label: NUTRA EFFECTS RADIANCE DAY CREAM SPF20 cream
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-9500-1, 10096-9500-2 - Packager: New Avon LLC
- 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 26, 2018
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
- For sunscreen use:
- apply generously and evenly 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
- product may stain fabrics
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INACTIVE INGREDIENT
Inactive Ingredients/Ingrédients inactifs: WATER/EAU, DIMETHICONE, GLYCERIN, PEG-8, CETEARYL ALCOHOL, TRISILOXANE, BEHENYL ALCOHOL, BUTYLOCTYL SALICYLATE, DILAURYL THIODIPROPIONATE, SILICA, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, PHENOXYETHANOL, CARBOMER, CETEARETH-20, THIODIPROPIONIC ACID, CAPRYLYL GLYCOL, DIMETHICONE CROSSPOLYMER, SODIUM HYDROXIDE, ISOHEXADECANE, DISODIUM EDTA, FRAGRANCE/PARFUM, PASSIFLORA INCARNATA SEED OIL, POLYSORBATE 60, PANTHENOL, TOCOPHERYL ACETATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, SALVIA HISPANICA SEED EXTRACT.
- QUESTIONS
- PACKAGE LABEL
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INGREDIENTS AND APPEARANCE
NUTRA EFFECTS RADIANCE DAY CREAM SPF20
nutra effects radiance day cream spf20 creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-9500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 3.5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 3 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.5 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:10096-9500-2 1 in 1 CARTON 01/01/2017 1 NDC:10096-9500-1 50 g in 1 JAR; 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)
