C and C by Clean and Clear Black Out Blackhead Clearing Coffee Scrub: Package Insert and Label Information

C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB- 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.

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)

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)

Principal Display Panel -- 124 mL Tube Label
(click image for full-size original)
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 DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Salicylic Acid (Salicylic Acid) Salicylic Acid 20 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
Water
Cocamidopropyl Hydroxysultaine
Sodium C14-16 Olefin Sulfonate
Sorbitol
Powdered Cellulose
Edetate Disodium Anhydrous
C12-15 Alkyl Lactate
Benzalkonium Chloride
Sodium Hydroxide
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate
Microcrystalline Wax
Menthol, Unspecified Form
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69968-0346-4 124 mL in 1 TUBE None
2 NDC:69968-0346-1 30 mL in 1 TUBE None
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)

Revised: 04/2018 Johnson & Johnson Consumer Inc.

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