Label: CANAFARMA SPOT ON ACNE TREATMENT- salicylic acid cream
- NDC Code(s): 80818-246-01
- 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:
- Clean the 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.
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INACTIVE INGREDIENTS:
Inactive ingredients: Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butylene Glycol, Butyrospermum Parkii (Shea) Butter, Cannabis Sativa (European Hemp) Oil, Cetearyl Alcohol, Cetearyl Glucoside, Cetyl Alcohol, Chamomilla Recutita (Chamomile) Extract, DMAE Bitartrate, Dimethicone, Fucus Vesiculosus (Seaweed) Extract, Glycerin, Glycyrrhiza Glabra (Licorice) Extract, Hydrogen Peroxide, Melaleuca Alternifolia (Tea Tree) Oil, Mentha Piperita (Peppermint) Oil, Methylisothiazolinone, Polysorbate-20, Retinol (Vitamin A), Salix Alba (Willow) Bark Extract, Sodium Hydroxide, Sodium PCA, Sodium Pyrophosphate, Tocopheryl Acetate (Vitamin E), Xanthan Gum
- OTHER INFORMATION:
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
CANAFARMA SPOT ON ACNE TREATMENT
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80818-246 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 ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SHEA BUTTER (UNII: K49155WL9Y) CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETYL ALCOHOL (UNII: 936JST6JCN) CHAMOMILE (UNII: FGL3685T2X) DEANOL BITARTRATE (UNII: D240J05W14) DIMETHICONE (UNII: 92RU3N3Y1O) FUCUS VESICULOSUS (UNII: 535G2ABX9M) GLYCERIN (UNII: PDC6A3C0OX) LICORICE (UNII: 61ZBX54883) HYDROGEN PEROXIDE (UNII: BBX060AN9V) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) TEA TREE OIL (UNII: VIF565UC2G) PEPPERMINT OIL (UNII: AV092KU4JH) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) POLYSORBATE 20 (UNII: 7T1F30V5YH) RETINOL (UNII: G2SH0XKK91) SALIX ALBA BARK (UNII: 205MXS71H7) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80818-246-01 29.6 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)
