WALGREENS SCAR CREAM W/SPF 30- avobenzone3%,octocrylene10%,oxybenone 6% cream

Walgreens Scar Cream w/SPF 30 by

Drug Labeling and Warnings

Walgreens Scar Cream w/SPF 30 by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Avobenzone 3%

Octocrylene 10%

Oxybenzone 6%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunburn

WARNINGS

For External use only

Do not use on: Damaged or broken skin

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Keep out of eyes

Rinse with water to remove

Stop use and ask a doctor:

If rash occurs

DOSAGE & ADMINISTRATION

For Sunscreen use: Apply liberally 15 minutes before exposure

Reapply at least 2 hours

Children under 6 months : Ask a doctor

Use a water - resistant sunscreen if swimming or sweating

OTHER SAFETY INFORMATION

Store at room temperature

Protect this product from excessive heat and direct sun

INACTIVE INGREDIENT

Allium Cepa (Onion) Bulb Extract, Ammonium Acryloyl- Dimethyltaurate/VP Copolymer, C12-15 Alkyl Benzoate, Capryl/Capric Triglyceride, Ceramide NG, Dicaprylyl Carbonate, Disodium EDTA, Fragrance, Glycerin, Hyrogenated Lechithin, Pentylene Glycol, Phenoxyethanol, SD Alcohol 40 B, Shea Butter, Sodium Hyaluronate, Squalane, Water, Xanthan Gum

QUESTIONS

1-800-925-4733

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS SCAR CREAM W/SPF 30 
avobenzone3%,octocrylene10%,oxybenone 6% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-2054
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	60 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DEHYDRATED ALCOHOL (UNII: 3K9958V90M)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ONION (UNII: 492225Q21H)
CERAMIDE NG (UNII: C04977SRJ5)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
SHEA BUTTER (UNII: K49155WL9Y)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
SQUALANE (UNII: GW89575KF9)
XANTHAN GUM (UNII: TTV12P4NEE)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-2054-01	28 g in 1 TUBE; Type 0: Not a Combination Product	04/29/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	04/29/2022

Labeler - Walgreens (008965063)