SAFEWAY SIGNATURE CARE NO BREAKOUT SUNSCREEN FACE SPF 30- avobenzone, homosalate, octisalate, octocrylene lotion

Safeway Signature Care No Breakout Sunscreen Face SPF 30 by

Drug Labeling and Warnings

Safeway Signature Care No Breakout Sunscreen Face SPF 30 by is a Otc medication manufactured, distributed, or labeled by Safeway, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 2.5%, Homosalate 6.0%, Octisalate 4.0%, Octocrylene 3.0%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early aging caused by the sun

Warnings

For external use only

Do not use on

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

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

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

water, tridecyl salicylate, silica, styrene acrylates copolymer, C12-15 alkyl benzoate, cetyl dimethicone, dimethicone, acrylates/dimethicone copolymer, phenoxyethanol, xanthan gum, steareth-100, steareth-2, adipic acid/diglycol crosspolymer, caprylyl glycol, sodium polyacrylate, glycerin, ethylhexylglycerin, ethylhexyl stearate, disodium EDTA, trideceth-6, bisabolol, mannan, propylene glycol, butylene glycol, capryloyl glycine, cedrus atlantica bark extract, hexylene glycol, sarcosine, portulaca oleracea extract, cinnamomum zeylancium bark extract, chlorphenesin.

Label

INGREDIENTS AND APPEARANCE

SAFEWAY SIGNATURE CARE NO BREAKOUT SUNSCREEN FACE SPF 30 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21130-753
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	60 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
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
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: 21130-753-03	88 mL in 1 TUBE; Type 0: Not a Combination Product	10/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/15/2019	02/21/2025

Labeler - Safeway, Inc. (009137209)