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.

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

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

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0346-4	124 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2018	05/31/2021
2	NDC:69968-0346-1	30 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2018	05/31/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part333D	06/01/2018	05/31/2021

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.