WALGREENS SPF 60 MELT-IN MILK SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene lotion

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 7%

PURPOSE

Sunscreen

INDICATIONS & USAGE

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 avoid contact wth eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritaton develops and lasts.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Apply liberally 15 minutes before sun exposure and as needed. 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 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
• Children under 6 months of age: ask a doctor

INACTIVE INGREDIENT

Water, Butyloctyl salicylate, styrene/acrylates copolymer, dimethicone, polymethylsilsesquioxane, caprylyl methicone, glycerin, poly C10-30 alkyl acrylate, inulin lauryl carbamate, acrylates/dimethicone copolymer, diethylhexyl syringylidenemalonate, PEG-100 stearate, glyceryl stearate, phenoxyethanol, potassium cetyl phosphate, propylene glycol, caprylyl glycol, alchol denat., acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, tocopherol, disodicum EDTA, p-anisic acid, caprylic/capric triglyceride, xanthan gum, cassia alata leaf extract, malto dexttrin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS SPF 60 MELT-IN MILK SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-8129
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	7 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIMETHICONE 200 (UNII: RGS4T2AS00)
TROLAMINE (UNII: 9O3K93S3TK)
XANTHAN GUM (UNII: TTV12P4NEE)
SENNA ALATA LEAF (UNII: 4BXR6YZN92)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
WATER (UNII: 059QF0KO0R)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
GLYCERIN (UNII: PDC6A3C0OX)
BEHENYL ACRYLATE POLYMER (UNII: D64PM5UT4U)
INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)
P-ANISIC ACID (UNII: 4SB6Y7DMM3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-8129-05	148 mL in 1 TUBE; Type 0: Not a Combination Product	11/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/14/2025

Labeler - Walgreens (008965063)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(0363-8129)