RE NUTRIV RADIANT UV BASE BROAD SPECTRUM SPF 50- homosalate , octyl salicylate, avobenzone, oxybenzone, octocrylene lotion
Drug Labeling and Warnings
Drug Details [pdf]
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS:
- PURPOSE
- USE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- SPL UNCLASSIFIED SECTION
-
DIRECTIONS
For sunscreen use:
* apply liberally 15 minutes before sun exposure
* reapply at least every two 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:
o limit time in the sun, especially from 10 a.m.–2 p.m.
o wear long-sleeved shirts, pants, hats and sunglasses
* children under 6 months of age: ask a doctor -
INACTIVE INGREDIENTS
WATER\AQUA\EAU [] BUTYLOCTYL SALICYLATE [] METHYL TRIMETHICONE [] NEOPENTYL GLYCOL DIHEPTANOATE [] ALEURITES MOLUCCANA (KUKUI) SEED OIL [] LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE [] PEG-100 STEARATE [] BUTYLENE GLYCOL [] DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE [] GLYCERYL STEARATE [] ALGAE EXTRACT [] LAMINARIA OCHROLEUCA EXTRACT [] LAMINARIA DIGITATA EXTRACT [] CETYL ALCOHOL [] CAFFEINE [] HYDROLYZED WHEAT PROTEIN [] VP/EICOSENE COPOLYMER [] PEARL POWDER [] GOLD [] SODIUM HYALURONATE [] ERGOTHIONEINE [] STEARIC ACID [] DEHYDROXANTHAN GUM [] POTASSIUM CETYL PHOSPHATE [] ETHYLHEXYLGLYCERIN [] AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER [] SACCHARIDE ISOMERATE [] CAPRYLYL GLYCOL [] GLYCERIN [] SORBITOL [] SILICA [] CAPRYLIC/CAPRIC TRIGLYCERIDE [] FRAGRANCE (PARFUM) [] DISODIUM EDTA [] CITRIC ACID [] PHENOXYETHANOL [] SODIUM DEHYDROACETATE [] MICA [] TITANIUM DIOXIDE (CI 77891) [] RED 33 (CI 17200) [] BLUE 1 (CI 42090)
- OTHER INFORMATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RE NUTRIV RADIANT UV BASE BROAD SPECTRUM SPF 50
homosalate , octyl salicylate, avobenzone, oxybenzone, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 11559-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 5.0 mL in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5.0 mL in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3.0 mL in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 3.0 nmol in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.7 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) KUKUI NUT (UNII: J87WJ3E7VW) PEG-100 STEARATE (UNII: YD01N1999R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) NORI (UNII: 477TV3P5UX) LAMINARIA DIGITATA (UNII: 15E7C67EE8) CETYL ALCOHOL (UNII: 936JST6JCN) CAFFEINE (UNII: 3G6A5W338E) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) CALCIUM CARBONATE (UNII: H0G9379FGK) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ERGOTHIONEINE (UNII: BDZ3DQM98W) STEARIC ACID (UNII: 4ELV7Z65AP) XANTHAN GUM (UNII: TTV12P4NEE) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) SACCHARIDE ISOMERATE (UNII: W8K377W98I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) SORBITOL (UNII: 506T60A25R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) EDETATE DISODIUM (UNII: 7FLD91C86K) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 11559-017-01 1 in 1 CARTON 1 NDC: 11559-017-02 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/01/2012 Labeler - ESTEE LAUDER INC (005914387) Establishment Name Address ID/FEI Business Operations Len-Ron Manufacturing Division of Aramis Inc. 809771152 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Inc 042918826 manufacture Establishment Name Address ID/FEI Business Operations Northtec Keystone 949264774 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Northtec Bristol 959338336 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Northtec Keystone 943871157 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Estee Lauder Pennsylvania Distribution Center 2 828534516 manufacture, relabel, repack Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Ltd. 205952385 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics, Ltd. 244669714 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics, Ltd. 253616536 manufacture Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Distribution Centre 208579636 repack, relabel Establishment Name Address ID/FEI Business Operations ELGC K.K. 712808195 relabel, repack Establishment Name Address ID/FEI Business Operations Estee Lauder N.V. 370151326 manufacture Establishment Name Address ID/FEI Business Operations Whitman Laboratories Ltd. 216866277 manufacture Establishment Name Address ID/FEI Business Operations Aveda Corporation 071352058 manufacture Establishment Name Address ID/FEI Business Operations Pennsylvania Logistics Center (PALC) 078364654 repack, relabel
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