Label: MASK RX- salicylic acid cream
- NDC Code(s): 70317-004-15
- Packager: Remeverse
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 16, 2024
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- Mask RX Active ingredients
- Inactive Ingredients
- Directions
- Use
- Stop use section
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Warnings
For external use only
Do not use this medication if you have very sensiteive skin - are sensitive to Salicylic Acid.
Ask a doctor or a pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product.
When using this product - Avoid unnecessary sun exposure and use a sunscreen - Avoid contact with eyes, lips and mouth. - Skin irritation and dryness is more likely to occur if you use another topical acne medication at a time. Avoid contact with hair and dyed fabrics, which may be reduced by using this product less frequently or in a lower concentration.
Stop use and ask a doctor if skin irritation becomes severe.
- Mask RX
- Warning - keep out of the reach of children.
- Mask RX Label
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INGREDIENTS AND APPEARANCE
MASK RX
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70317-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.225 g in 15 g Inactive Ingredients Ingredient Name Strength CERAMIDE 3 (UNII: 4370DF050B) POLYSORBATE 20 (UNII: 7T1F30V5YH) ALOE (UNII: V5VD430YW9) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HYALURONIC ACID (UNII: S270N0TRQY) SHEA BUTTER (UNII: K49155WL9Y) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) ISODODECANE (UNII: A8289P68Y2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70317-004-15 15 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 09/01/2020 Labeler - Remeverse (050186540) Registrant - Lexia LLC (015552120) Establishment Name Address ID/FEI Business Operations Lexia LLC 015552120 manufacture(70317-004)