Rapid Clear 2 in 1 Fight & Fade Gel

Neutrogena Rapid Clear 2 in 1 Fight and Fade by

Drug Labeling and Warnings

Neutrogena Rapid Clear 2 in 1 Fight and Fade by is a Otc medication manufactured, distributed, or labeled by Neutrogena Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE - salicylic acid lotion 
Johnson & Johnson Consumer Inc.

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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Rapid Clear 2 in 1 Fight & Fade Gel

Drug Facts

Active Ingredient

Salicylic Acid 2%

Purpose

Acne treatment

Use

For the treatment of acne.

Warnings

For external use only

Flammable – Keep away from open fire or flame

Ask a doctor or pharmacist before use if you are using other topical acne medications at the 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.

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

Directions

• Cleanse the skin thoroughly before applying medication.
• Cover the entire affected area with a thin layer one to three times daily. Because 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 every other day.

Inactive ingredients

Alcohol Denat. (38%)
Hamamelis Virginiana (Witch Hazel) Water
Water
Polyquaternium-37
Glycerin
Glycolic Acid
Butylene Glycol
Cyclohexasiloxane
C12-15 Alkyl Lactate
Isodecyl Laurate
Cyclopentasiloxane
Cetyl Lactate
Polysorbate 20
Portulaca Oleracea Extract
Sodium Benzotriazolyl Butylphenol Sulfonate
Cocamidopropyl PG-Dimonium Chloride Phosphate
Sodium Hydroxide
Sodium Chloride
Bisabolol
Benzalkonium Chloride
Yellow 6
Red 40
Fragrance

Questions or comments?

(USA only) 1-800-584-4048 or www.neutrogena.com

Sun Alert

This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards.

© Dist. by Neutrogena Corp., L.A., CA 90045

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

NEUTROGENA
Rapid
Clear®

2-in-1
Fight & Fade Gel

MICROCLEAR™
Technology
Reduces breakouts in 8 hours
Neutrogena®

Salicylic acid acne treatment

0.5 FL OZ (15mL)

NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE  
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-286
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
Witch Hazel (UNII: 101I4J0U34)
POLYQUATERNIUM-37 (25000 MPA.S) (UNII: 31L31U8285)
Glycerin (UNII: PDC6A3C0OX)
Glycolic Acid (UNII: 0WT12SX38S)
Butylene Glycol (UNII: 3XUS85K0RA)
Cyclomethicone 6 (UNII: XHK3U310BA)
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
ISODECYL LAURATE (UNII: 254BX4O0JU)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Cetyl Lactate (UNII: A7EVH2RK4O)
Polysorbate 20 (UNII: 7T1F30V5YH)
Purslane (UNII: M6S840WXG5)
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
Sodium Hydroxide (UNII: 55X04QC32I)
Sodium Chloride (UNII: 451W47IQ8X)
Levomenol (UNII: 24WE03BX2T)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Fd&C Yellow No. 6 (UNII: H77VEI93A8)
FD&C Red No. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-286-01	1 in 1 CARTON	12/23/2011	12/15/2016
1		15 mL 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	12/23/2011	12/15/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2019

Document Id: 8f06a991-098c-47c5-9e3b-f654d6808103

34390-5

Set id: 856c4255-4458-4879-a4a8-e42e88242dbd

Version: 2

Effective Time: 20191216

 

Johnson & Johnson Consumer Inc.