CLEAR DAYS AHEAD FAST-ACTING SALICYLIC ACID ACNE SPOT TREATMENT- salicylic acid gel

clear days ahead by

Drug Labeling and Warnings

clear days ahead by is a Otc medication manufactured, distributed, or labeled by Philosophy, Process Technologies and Packaging Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic Acid (2.0%)

Purpose

Acne Treatment

Indications

• for the treatment of acne

Warnings

For external use only

Ask a doctor or pharmacist before using if you are using other topical acne medications at he same time or immediately following use of this product. this may increase dryness or irritation of the skin. if this occurs, only one medication should be used unless directed by a doctor.

When using this product

• avoid contact with eyes. If contact occurs, flush thoroughly with water. If redness or irritation persists, contact your doctor right away.

Keep out of reach of children.

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

Directions

• cleanse skin thoroughly before applying medication. cover the entire affected area with a thin layer 1-3 times daily
• because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2-3 times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive ingredients

water, dimethicone, isododecane, polysilicone-11, alcohol denat., hexyldecanol, glycolic acid, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, coco-caprylate/caprate, squalane, bisabolol, butylene glycol, cetylhydroxyproline palmitamide, ethylhexylglycerin, lecithin, oligopeptide-10, trimethylpentanediol/ adipic acid copolymer, rassica campestris (rapeseed) sterols, laureth-12, polysorbate 60, decyl glucoside, lauryl glucoside, stearic acid, sodium acrylates copolymer, ethoxydiglycol, sodium hydroxide, disodium edta, aprylyl glycol, hexylene glycol, phenoxyethanol, o-cymen-5-ol.

Questions or comments?

Call toll-free 1-800-568-3151 from 8a.m. - 5p.m. MST

(Monday - Friday)

Principal Display Panel - 15 ml Bottle Label

clear

days ahead™

philosophy®: instead
of focusing on what is
wrong, focus on what
is right and watch your
days become clearer

fast-acting salicylic acid

acne spot treatment

15 ml/0.5 fl oz.

Principal Display Panel - 15 ml Box Label

clear

days ahead™

philosophy®: a blemish
is “small stuff” and not
worth the worry time.
family, friends and your
health are the “big stuff”
that really matter. Instead
of focusing on what is
wrong, focus on what is
right and watch your days
become clearer.

fast-acting salicylic acid

acne spot treatment

15 ml/0.5 fl. oz.

INGREDIENTS AND APPEARANCE

CLEAR DAYS AHEAD   FAST-ACTING SALICYLIC ACID ACNE SPOT TREATMENT
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50184-1020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.3 g  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISODODECANE (UNII: A8289P68Y2)
HEXYLDECANOL (UNII: 151Z7P1317)
GLYCOLIC ACID (UNII: 0WT12SX38S)
SQUALANE (UNII: GW89575KF9)
LEVOMENOL (UNII: 24WE03BX2T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PALMITAMIDE (UNII: QX1MQ82M73)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
RAPESEED STEROL (UNII: B46B6DD20U)
LAURETH-12 (UNII: OAH19558U1)
POLYSORBATE 60 (UNII: CAL22UVI4M)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
O-CYMEN-5-OL (UNII: H41B6Q1I9L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50184-1020-1	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2012
2	NDC: 50184-1020-2	15 mL in 1 BOX; Type 0: Not a Combination Product	04/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	04/01/2012

Labeler - Philosophy (948102256)

Establishment
Name	Address	ID/FEI	Business Operations
Process Technologies and Packaging Inc.		809172885	manufacture(50184-1020)