WELL AT WALGREENS ULTIMATE DAILY- salicylic acid gel

Well at Walgreens by

Drug Labeling and Warnings

Well at Walgreens by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid  2.0%

PURPOSE

Purpose

Acne Treatment

INDICATIONS & USAGE

Uses

for the treatment of acne

WARNINGS

Warnings

For external use only

WHEN USING

When using this product

-skin irritation and dryness is more likely to occur

if you use another topical acne medication at the

same time. If irritation occurs, only use one topical

acne medication at a time.

Avoid contact with eyes. If contact occurs, flush

thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get

medical help or contact a Poison Control Center right

away.

DOSAGE & ADMINISTRATION

Directions

-wet face

-dispense product into hands and massage gently

onto face and neck, avoiding the delicate eye area.

-rinse thoroughly with warm water and pay dry

-for best results, use twice a day.

INACTIVE INGREDIENT

Inactive ingredients butylparaben, caramel, cetearyl alcohol,

cistus monspeliensis extract, disodium EDTA, DMDM

hydantoin, ethylparaben, fragrance, glycerin, heluchrysum

italicum extract, isobutylparaben, laureth-3, lavandula stoechas

extract, methylparaben, phenoxyethanol, propylparaben,

sodium cocoyl isethionate, sodium hydroxide, stearic acid, water

QUESTIONS

Questions or comments?  1-800-925-4733

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WELL AT WALGREENS  ULTIMATE DAILY
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-3400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	4 g  in 200 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLPARABEN (UNII: 3QPI1U3FV8)
CARAMEL (UNII: T9D99G2B1R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CISTUS MONSPELIENSIS LEAF (UNII: 1IE70KNO43)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ETHYLPARABEN (UNII: 14255EXE39)
GLYCERIN (UNII: PDC6A3C0OX)
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
LAURETH-3 (UNII: F32E4CB0UJ)
LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-3400-15	200.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/01/2015

Labeler - Walgreen Company (008965063)