C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB- salicylic acid lotion

C and C by Clean and Clear black out blackhead clearing coffee scrub by

Drug Labeling and Warnings

C and C by Clean and Clear black out blackhead clearing coffee 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 ingredient

Salicylic Acid (2%)

Purpose

Acne medication

Use

• 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

massage onto damp face, avoiding eyes. rinse thoroughly. use daily.

Other Information

store at room temperature

Inactive ingredients

Water, Cocamidopropyl Hydroxysultaine, Sodium C14-16 Olefin Sulfonate, Sorbitol, Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Fragrance, Sodium Hydroxide, Microcrystalline Wax, Menthol, Disodium EDTA, C12-15 Alkyl Lactate, Benzalkonium Chloride, Cocamidopropyl PG-Dimonium Chloride Phosphate

Questions?

call toll-free 1-877-754-6411 or 215-273-8755 (collect)

SPL UNCLASSIFIED SECTION

Distributed by:
Johnson & Johnson Consumer Inc.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

C&C
by Clean & Clear

black
out

blackhead clearing
coffee scrub
salicylic acid acne medication

4.2 fl oz (124mL)

INGREDIENTS AND APPEARANCE

C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0346
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)
Cocamidopropyl Hydroxysultaine (UNII: 62V75NI93W)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Sorbitol (UNII: 506T60A25R)
Powdered Cellulose (UNII: SMD1X3XO9M)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
C12-15 Alkyl Lactate (UNII: GC844VRD7E)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Sodium Hydroxide (UNII: 55X04QC32I)
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)
Microcrystalline Wax (UNII: XOF597Q3KY)
Menthol, Unspecified Form (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0346-4	124 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2018
2	NDC: 69968-0346-1	30 mL 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	06/01/2018

Labeler - Johnson & Johnson Consumer Inc. (002347102)