SHEER TOUCH SUNSCREEN SPF 55- avobenzone, homosalate, octisalate lotion

Sheer Touch Sunscreen SPF 55 by

Drug Labeling and Warnings

Sheer Touch Sunscreen SPF 55 by is a Otc medication manufactured, distributed, or labeled by Amazon.com Services LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3%

Homosalate 12%

Octisalate 5%

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 skin aging caused by the sun

Warnings

For external use only

Do not use

• 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 right away.

Directions

• apply liberaly 15 minutes before sun exposure
• apply to all skin exposed to the sun
• 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• limit time in the sun, especialy from 10  a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect the product in this container from excessive heat and direct sun

Inactive ingredients

water, diethylhexyl 2,6-naphthalate, styrene/acrylates copolymer, silica, butyloctyl salicylate, glyceryl stearate, PEG-100 stearate, dimethicone, potassium cetyl phosphate, benzyl alcohol, beeswax, caprylyl methicone, cetyl dimethicone, aluminum starch octenylsuccinate, behenyl alcohol, acrylates/C12-22 alkyl methacrylate copolymer, xanthan gum, sodium polyacrylate, chlorphenesin, dimethicone/PEG-10/15 crosspolymer, fragrance, ethylhexyl stearate, glycerin, disodium EDTA, tocopheryl acetate, BHT, trideceth-6, pentylene glycol, benzyl benzoate

Disclaimer

*This product is not manufacturedor distributed by Kenvue, Inc., distributor of Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 55.

May stain or damage some fabrics or surfaces.

Adverse Reaction

Dist. by: Amazon.com Services, LLC

Seattle, WA 98109 1-877-485-0385

© 2023 Amazon.com, Inc or its affiliates. All rights reserved.

www.amazon.com/amazonbasics

Principal panel Display

amazon basics

sheer touchsunscreen lotion

Broad Spectrum SPF 55

Water Resistant (80 minutes)

Dermatologist Tested

Formulated Without Octinoxate, Oxybenzone, & Octocrylene

Compare to Neutrogene Broad Spectrum SPF 55*

SPF 55

3 FL OZ (88 mL)

INGREDIENTS AND APPEARANCE

SHEER TOUCH SUNSCREEN SPF 55 
avobenzone, homosalate, octisalate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72288-933
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	120 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
DIMETHICONE (UNII: 92RU3N3Y1O)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
BENZYL ALCOHOL (UNII: LKG8494WBH)
YELLOW WAX (UNII: 2ZA36H0S2V)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
DOCOSANOL (UNII: 9G1OE216XY)
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CHLORPHENESIN (UNII: I670DAL4SZ)
DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
BENZYL BENZOATE (UNII: N863NB338G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72288-933-21	88 mL in 1 TUBE; Type 0: Not a Combination Product	12/27/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/27/2023

Labeler - Amazon.com Services LLC (128990418)

Registrant - Vi-Jon, LLC (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		790752542	manufacture(72288-933)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, LLC		088520668	manufacture(72288-933)