Label: MEIJER SPF 30 FACE- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
- NDC Code(s): 41250-967-03
- Packager: MEIJER DISTRIBUTION, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 October 3, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- DO NOT USE
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
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Directions
- apply liberally 15 minutes before sun exposure
- Reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- children under 6 months of age: Ask a doctor
- 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
-
Inactive ingredients
water, silica, styrene acrylates copolymer, cetyl dimethicone, C12-15 alkyl benzoate, dimethicone, acrylates/dimethicone copolymer, phenoxyethanol, xanthan gum, steareth-100, steareth-2, adipic acid/diglycol crosspolymer, caprylyl glycol, sodium polyacrylate, ethylhexylglycerin, glycerin, ethylhexyl stearate, BHT, disodium EDTA, trideceth-6, bisabolol, mannan, propylene glycol, butylene glycol, capryloyl glycine, hexylene glycol, cedrus atlantica bark extract, sarcosine, portulaca oleracea extract, cinnamomum zeylancium bark extract, chlorphenesin.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEIJER SPF 30 FACE
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-967 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 40 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 30 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CINNAMON BARK OIL (UNII: XE54U569EC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PURSLANE (UNII: M6S840WXG5) CHLORPHENESIN (UNII: I670DAL4SZ) ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19) GLYCERIN (UNII: PDC6A3C0OX) ACRYLIC ACID (UNII: J94PBK7X8S) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TRIDECETH-6 (UNII: 3T5PCR2H0C) LEVOMENOL (UNII: 24WE03BX2T) KONJAC MANNAN (UNII: 36W3E5TAMG) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) STEARETH-100 (UNII: 4OH5W9UM87) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) STEARETH-2 (UNII: V56DFE46J5) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SARCOSINE (UNII: Z711V88R5F) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) XANTHAN GUM (UNII: TTV12P4NEE) CETYL DIMETHICONE 45 (UNII: IK315POC44) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-967-03 88 mL in 1 TUBE; Type 0: Not a Combination Product 10/10/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 10/10/2018 Labeler - MEIJER DISTRIBUTION, INC (006959555)