Label: CANAFARMA SPOT ON ACNE TREATMENT CLEANSER- salicylic acid cream
- NDC Code(s): 80818-245-04
- Packager: Canafarma Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- DRUG FACTS
- ACTIVE INGREDIENTS
- USES:
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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.
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DIRECTIONS:
- Use every morning and evening
- Wet area first.
- Apply a dime sized amount to palm and create a lather.
- Gently massage over the face and neck
- Rinse well.
- May also be used on chest and back.
- 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.
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INACTIVE INGREDIENTS:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Cannabis Sativa (European Hemp) Oil, Chamomilla Recutita (Chamomile) Extract, Citrus Grandis (Grapefruit) Seed Extract, Cocamidopropyl Betaine, Disodium Oleamido MEA Sulfosuccinate, Ethylhexylglycerin, Fucus Vesiculosus (Seaweed) Extract, Glycerin, Glycol Stearate, Glycolic Acid, Guar Hydroxypropyltrimonium Chloride, Melaleuca Alternifolia (Tea Tree) Oil, Mentha Piperita (Peppermint) Oil, Mentha Viridis (Spearmint) Oil, Phenoxyethanol, Rosa Canina (Rose) Hips Oil, Sodium Hydroxide, Sodium Laureth Sulfate, Sodium Lauryl Sulfate.
- OTHER INFORMATION:
- QUESTIONS?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
CANAFARMA SPOT ON ACNE TREATMENT CLEANSER
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80818-245 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D) CHAMOMILE (UNII: FGL3685T2X) CITRUS MAXIMA SEED (UNII: 083X55C543) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DISODIUM OLEAMIDO MONOETHANOLAMINE SULFOSUCCINATE (UNII: 5M1101WGSY) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) FUCUS VESICULOSUS (UNII: 535G2ABX9M) GLYCERIN (UNII: PDC6A3C0OX) GLYCOL STEARATE (UNII: 0324G66D0E) GLYCOLIC ACID (UNII: 0WT12SX38S) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) TEA TREE OIL (UNII: VIF565UC2G) PEPPERMINT OIL (UNII: AV092KU4JH) SPEARMINT (UNII: J7I2T6IV1N) PHENOXYETHANOL (UNII: HIE492ZZ3T) ROSA CANINA FRUIT (UNII: 3TNW8D08V3) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80818-245-04 118.29 mL in 1 TUBE; Type 0: Not a Combination Product 10/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2020 Labeler - Canafarma Corp. (117670069)
