Drug Labeling and Warnings

Drug Details

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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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 Bottle Label

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.

Principal Display Panel - 15 ml Box Label
CLEAR DAYS AHEAD   FAST-ACTING SALICYLIC ACID ACNE SPOT TREATMENT
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 50184-1020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.3 g  in 15 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 50184-1020-115 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2012
2NDC: 50184-1020-215 mL in 1 BOX; Type 0: Not a Combination Product04/01/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D04/01/2012
Labeler - Philosophy (948102256)
Establishment
NameAddressID/FEIBusiness Operations
Process Technologies and Packaging Inc.809172885manufacture(50184-1020)

Revised: 2/2019
 
Philosophy


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