NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- salicylic acid gel

Neutrogena Rapid Clear Acne Eliminating Spot by

Drug Labeling and Warnings

Neutrogena Rapid Clear Acne Eliminating Spot by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Medication

Use

For the treatment of acne.

Warnings

For external use only.

Flammable

Keep away from fire or flame.

When using this product

• skin irritation and dryness is more likely to occour if you use another tropical acne medication at the same time. If irritation occurs, only use one topical medication at a time

• if eye 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 product.
• cover the entire affected area with a thin layer 1-3 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.

Other information

Sunburn 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 a protective clothing, and limit sun exposure while using this product and for a week afterwards. Store at Room Temperature.

Inactive ingredients

water, alcohol denat., hamamelis virginiana (witch hazel) water, polyacrylamide, glycerin, cyclopentasiloxane, C13-14 isoparaffin, C12-15 alkyl lactate, alcohol, phenoxyethanol, cetyl lactate, PPG-2 isoceteth-20 acetate, cocamidopropyl PG-dimonium chloride phosphate, laureth-7, polysorbate 20, phenethyl dimethicone, fragrance, dehydroxanthan gum, propylene glycol, benzalkonium chloride, ammonia, tetrasodium EDTA, butylene glycol, capryloyl glycine, sarcosine, cinnamomum zeylanicum bark extract, cedrus atlantica bark extract, portulaca oleracea extract

Questions?

800-299-4786; Outside US dial collect US, 215-273-8755 or www.neutrogena.com

SPL UNCLASSIFIED SECTION

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

NEW LOOK

NEUTROGENA
Rapid
Clear®

Acne
Eliminating
Spot Gel

MICROCLEAR®
technology

Neutrogena®

salicylic acid acne treatment

0.5 FL OZ (15mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0472
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)
hamamelis virginiana top water (UNII: NT00Y05A2V)
glycerin (UNII: PDC6A3C0OX)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
C13-14 isoparaffin (UNII: E4F12ROE70)
C12-15 alkyl lactate (UNII: GC844VRD7E)
alcohol (UNII: 3K9958V90M)
phenoxyethanol (UNII: HIE492ZZ3T)
cetyl lactate (UNII: A7EVH2RK4O)
PPG-2 isoceteth-20 acetate (UNII: BI6C7YO419)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
LAURETH-7 (UNII: Z95S6G8201)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
benzalkonium chloride (UNII: F5UM2KM3W7)
ammonia (UNII: 5138Q19F1X)
EDETATE SODIUM (UNII: MP1J8420LU)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
sarcosine (UNII: Z711V88R5F)
cinnamon bark oil (UNII: XE54U569EC)
cedrus atlantica bark (UNII: ITP1Q41UPF)
purslane (UNII: M6S840WXG5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0472-1	1 in 1 CARTON	10/30/2019
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	10/30/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)