6110,6117 Paulas Choice Clear Daily Skin Clearing Treatment 5% Benzoyl Peroxide Extra Strength

Paulas Choice Clear Daily Skin Clearing Treatment by

Drug Labeling and Warnings

Paulas Choice Clear Daily Skin Clearing Treatment by is a Otc medication manufactured, distributed, or labeled by Paula's Choice. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PAULAS CHOICE CLEAR DAILY SKIN CLEARING TREATMENT- benzoyl peroxide lotion 
Paula's Choice

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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6110,6117 Paulas Choice Clear Daily Skin Clearing Treatment 5% Benzoyl Peroxide Extra Strength

For the treatment of Acne

Penetrates pores to control acne blemishes, blackheads and whiteheads.

Helps prevent new acne blemishes, blackheads and whiteheads.

For external use only.

Do not use if you:

- Have very sensitive skin

-Are sensitive to benzoyl peroxide.

- Skin irritation and dryness is more likely to occur if you use another topical medication at the same time.

-If irritation occurs, only use one topical acne medication at a time

-Avoid unnecessary sun expossure

-Avoid contact with the eyes, lip and mouth

Avoid contact with hair and dyed fabrics, which may be bleached by this product

SKin irritation may occur, characterized by redness, burning , itching, peling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask doctor if skin irritation occurs or get worse.

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Apply after cleansing and exfoliating.

Cover the entire affected area with a thin layer one to three times daily

Because excessive drying of the skin may occur, start wit oe application daily, then gradually increase to two or three 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

If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Store at 20-25 degrees Celcius.

Water (Aqua), Propylene Glycol, Bisabolol, Allantoin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxyethylcellulose, Sodium Citrate, Laureth-4, Caprylyl Glycol, Sodium Hydroxide, Disodium EDTA, Hexylene Glycol, Phenoxyethanol.

Benzoyl Peroxide, 5.0%

For the treatment of acne. Penetrates pores to control acne blemishes, blackheads and whiteheads. Helps prevent new acne blemishesm blackheads and whiteheads.

- Apply after cleansing and exfoliating

-Cover the entir eaffected area with a thin layer one to three times daily

-Becase excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three 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

-If going outside, appy sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Benzoyl Peroxide, 2.5%

6110 Component Label

PAULAS CHOICE CLEAR DAILY SKIN CLEARING TREATMENT 
benzoyl peroxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76144-611
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
LAURETH-4 (UNII: 6HQ855798J)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
LEVOMENOL (UNII: 24WE03BX2T)  
WATER (UNII: 059QF0KO0R)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
ALLANTOIN (UNII: 344S277G0Z)  
CARBOMER 1342 (UNII: 809Y72KV36)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76144-611-0715 mL in 1 TUBE; Type 0: Not a Combination Product09/07/2012
2NDC: 76144-611-0067 mL in 1 TUBE; Type 0: Not a Combination Product09/07/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00609/07/2012
Labeler - Paula's Choice (029583981)

Revised: 12/2022
 

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