Kroger D34.000/D34AA Sheer Touch Sunscreen SPF 100

Sheer Touch Sunscreen SPF 100 by

Drug Labeling and Warnings

Sheer Touch Sunscreen SPF 100 by is a Otc medication manufactured, distributed, or labeled by Kroger Co., Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SHEER TOUCH SUNSCREEN SPF 100- avobenzone, homosalate, octisalate lotion 
Kroger Co.

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Kroger D34.000/D34AA
Sheer Touch Sunscreen SPF 100

Active ingredients

Avobenzone 3%

Homosalate 15%

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, butyloctyl salicylate, silica, glyceryl stearate, PEG-100 stearate, potassium cetyl phosphate, beeswax, behenyl alcohol, acrylates/C12-22 alkyl methacrylate copolymer, benzyl alcohol, fragrance, xanthan gum, chlorphenesin, sodium polyacrylate, glycerin, disodium EDTA, BHT, trideceth-6, pentylene glycol

Adverse Reaction

DISTRIBUTED BY THE KROGER CO

CINCINNATI, OHIO 45202

MAY STAIN OR DAMAGE SOME FABRICS OR SURFACES

Patent Pending

QUALITY GUARANTEE

800-632-6900

www.kroger.com

Principal display panel

Kroger ®

SHEER sunscreen lotion

BROAD SPECTRUM SPF 100

UVA/UVB SUNSCREEN

water resistant (80 mins)

UVA/UVB sunscreen

clean & lightweight feel

dermatologist-tested

SPF 100

3 FL OZ (88 mL)

image description

SHEER TOUCH SUNSCREEN SPF 100 
avobenzone, homosalate, octisalate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 59450-934
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
DOCOSANOL (UNII: 9G1OE216XY)  
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
GLYCERIN (UNII: PDC6A3C0OX)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 59450-934-2188 mL in 1 TUBE; Type 0: Not a Combination Product11/07/202306/25/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02011/07/202306/25/2024
Labeler - Kroger Co. (006999528)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(59450-934)

Revised: 8/2025
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