![C AND C BY CLEAN AND CLEAR SPOT ON SPOT TREATMENT (SALICYLIC ACID) LOTION [JOHNSON & JOHNSON CONSUMER INC.]](https://medic.hrt.org//dailymed/images/625f6318-a6be-4379-af32-0d605d3ee883/clean_n_clear-01.jpg)
| NDC | 69968-0347-1 |
| Set ID | 625f6318-a6be-4379-af32-0d605d3ee883 |
| 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
- if eye 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
- cleanse skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Other Information
- Sunburn Alert: this product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards.
- Inactive ingredients
Alcohol Denat., Water, Hamamelis Virginiana (Witch Hazel) Water, Polyacrylamide, Glycerin, Cyclopentasiloxane, C13-14 Isoparaffin, C12-15 Alkyl Lactate, Alcohol, Phenoxyethanol, Cetyl Lactate, PPG-2 Isoceteth-20 Acetate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laureth- 7, Polysorbate 20, Phenethyl Dimethicone, Fragrance, Dehydroxanthan Gum, Propylene Glycol, Benzalkonium Chloride, Ammonia, Tetrasodium EDTA, Butylene Glycol, Capryloyl Glycine, Sarcosine, Cinnamomum Zeylanicum Bark Extract, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract
Close - Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 14 mL Tube Carton
- INGREDIENTS AND APPEARANCE
C AND C BY CLEAN AND CLEAR SPOT ON SPOT TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0347 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) Alcohol (UNII: 3K9958V90M) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) Glycerin (UNII: PDC6A3C0OX) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) C13-14 Isoparaffin (UNII: E4F12ROE70) C12-15 Alkyl Lactate (UNII: GC844VRD7E) Polysorbate 20 (UNII: 7T1F30V5YH) PPG-2 Isoceteth-20 Acetate (UNII: BI6C7YO419) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) Laureth-7 (UNII: Z95S6G8201) Phenoxyethanol (UNII: HIE492ZZ3T) Dehydroxanthan Gum (UNII: 63ZP7I1BQO) Propylene Glycol (UNII: 6DC9Q167V3) Benzalkonium Chloride (UNII: F5UM2KM3W7) Ammonia (UNII: 5138Q19F1X) EDETATE SODIUM (UNII: MP1J8420LU) Butylene Glycol (UNII: 3XUS85K0RA) Capryloyl Glycine (UNII: 8TY5YO42NJ) Sarcosine (UNII: Z711V88R5F) CINNAMON BARK OIL (UNII: XE54U569EC) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) PURSLANE (UNII: M6S840WXG5) Cetyl Lactate (UNII: A7EVH2RK4O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0347-1 1 in 1 CARTON 06/01/2018 1 14 mL in 1 TUBE; Type 0: Not a Combination Product 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)
