CLEAN AND CLEAR BLACKHEAD ERASER SCRUB- salicylic acid cream

Clean and Clear blackhead eraser scrub by

Drug Labeling and Warnings

Clean and Clear blackhead eraser scrub 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 ingredients

Salicylic Acid 2%

Purpose

Acne treatment

Uses

• for the treatment of acne
• clears blackheads

Warnings

For external use only.

When using this product

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

• Wet face.
• Gently massage all over face for 20-30 seconds, avoiding eye area.
• Rinse thoroughly and pat dry.
• Recommended for daily use.

Other information

Store at Room Temperature.

Inactive ingredients

Water, Cetyl alcohol, PPG-15 Stearyl Ether, Cellulose, Glycerin, Polysorbate 60, Steareth-21, Microcrystalline Wax, Potassium Cetyl Phosphate, Xanthan Gum, Fragrance, Disodium EDTA, Methyl Lactate, Sodium Hydroxide, Ferric Ferrocyanide

Questions?

Call toll- free 877-754-6411 or 215-273-8755 (collect) or visit www.CleanandClear.com

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 198 g Tube Label

VALUE
SIZE

Clean
&
Clear®

blackhead
eraser®
scrub
salicylic acid acne medication

OIL-FREE

reduces the number
of blackheads

gently exfoliates to
lift away dirt & oil

Johnson & Johnson

NET WT. 7 OZ. (198 sg)

INGREDIENTS AND APPEARANCE

CLEAN AND CLEAR BLACKHEAD ERASER SCRUB 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0234
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 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cetyl Alcohol (UNII: 936JST6JCN)
PPG-15 Stearyl Ether (UNII: 1II18XLS1L)
Steareth-21 (UNII: 53J3F32P58)
Polysorbate 60 (UNII: CAL22UVI4M)
Powdered Cellulose (UNII: SMD1X3XO9M)
Glycerin (UNII: PDC6A3C0OX)
Microcrystalline Wax (UNII: XOF597Q3KY)
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)
Xanthan Gum (UNII: TTV12P4NEE)
Sodium Hydroxide (UNII: 55X04QC32I)
Edetate Disodium (UNII: 7FLD91C86K)
Methyl Lactate, (-)- (UNII: 0379G9C44S)
Ferric Ferrocyanide (UNII: TLE294X33A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0234-5	141 g in 1 TUBE; Type 0: Not a Combination Product	06/01/2016
2	NDC: 69968-0234-7	198 g in 1 TUBE; Type 0: Not a Combination Product	06/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	06/01/2016

Labeler - Johnson & Johnson Consumer Inc. (002347102)