Label: CLEAR SPF 30 FACE SUNSCREEN WEGMANS- avobenzone - 3.0% homosalate - 12.0% octisalate - 5.0% octocrylene - 3.0% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 47124-451-03 - Packager: Wegman
- 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 January 9, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients Purpose
- PURPOSE
- INDICATIONS & USAGE
- Warnings
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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
• 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 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-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor -
Inactive ingredients
Acrylates/Dimethicone Copolymer
BHT
Bisabolol
Butylene Glycol
C12-15 Alkyl Benzoate
Capryloyl Glycine
Caprylyl Glycol
Cedrus Atlantica Bark Extract
Cetyl Dimethicone
Chlorphenesin
Cinnamomum Zeylanicum Bark Extract
Cyclopentasiloxane
Disodium EDTA
Ethylhexyl Stearate
Ethylhexylglycerin
Mannan
Neopentyl Glycol Diheptanoate
Phenoxyethanol
Polyester-7
Polyester-8
Portulaca Oleracea Extract
Propylene Glycol
Sarcosine
Silica
Sodium Polyacrylate
Steareth-2
Steareth-100
Styrene/Acrylates Copolymer
Trideceth-6
Water
Xanthan Gum - Other information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEAR SPF 30 FACE SUNSCREEN WEGMANS
avobenzone - 3.0% homosalate - 12.0% octisalate - 5.0% octocrylene - 3.0% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47124-451 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) Avobenzone 3 g in 100 mL Homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) Homosalate 12 g in 100 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 5 g in 100 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 3 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) LEVOMENOL (UNII: 24WE03BX2T) Butylene Glycol (UNII: 3XUS85K0RA) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) Capryloyl Glycine (UNII: 8TY5YO42NJ) Caprylyl Glycol (UNII: 00YIU5438U) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) CINNAMON BARK OIL (UNII: XE54U569EC) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) EDETATE DISODIUM (UNII: 7FLD91C86K) Ethylhexyl Stearate (UNII: EG3PA2K3K5) Ethylhexylglycerin (UNII: 147D247K3P) YEAST MANNAN (UNII: 91R887N59P) Neopentyl Glycol Diheptanoate (UNII: 5LKW3C543X) Phenoxyethanol (UNII: HIE492ZZ3T) Polyester-7 (UNII: 0841698D2F) Propylene Glycol (UNII: 6DC9Q167V3) PURSLANE (UNII: M6S840WXG5) Sarcosine (UNII: Z711V88R5F) Steareth-2 (UNII: V56DFE46J5) Steareth-100 (UNII: 4OH5W9UM87) TRIDECETH-6 PHOSPHATE (UNII: NKT96BX1OC) Water (UNII: 059QF0KO0R) Xanthan Gum (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47124-451-03 89 mL in 1 TUBE; Type 0: Not a Combination Product 04/10/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/10/2013 Labeler - Wegman (059650069) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(47124-451) , label(47124-451)
