![C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB (SALICYLIC ACID) LOTION [JOHNSON & JOHNSON CONSUMER INC.]](https://medic.hrt.org//dailymed/images/16f5981f-379c-4446-8157-40623f47a090/blackout-01.jpg)
| NDC | 69968-0346-1, 69968-0346-4 |
| Set ID | 16f5981f-379c-4446-8157-40623f47a090 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Johnson & Johnson Consumer Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART333D |
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- 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
CloseKeep out of reach of children. if swallowed, get medical help or contact a Poison Control Center right away
- Directions
- Other Information
- 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
Close - Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
C&C
by Clean & Clearblack
outblackhead clearing
coffee scrub
salicylic acid acne medication4.2 fl oz (124mL)
Close
- INGREDIENTS AND APPEARANCE
C AND C BY CLEAN AND CLEAR BLACK OUT BLACKHEAD CLEARING COFFEE SCRUB
salicylic acid lotionProduct 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 CloseLabeler - Johnson & Johnson Consumer Inc. (002347102)