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.

----------

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

Drug Facts

Active ingredient

Salicylic Acid (2%)

Purpose

Acne medication

Use

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
C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0346
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0346-4124 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201805/31/2021
2NDC:69968-0346-130 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201805/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D06/01/201805/31/2021
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 6/2020
Document Id: d908003f-a5ca-49f7-b50e-f4da415c160a
Set id: 16f5981f-379c-4446-8157-40623f47a090
Version: 2
Effective Time: 20200624
 
Johnson & Johnson Consumer Inc.