Label: ACNE AND BLEMISH CONTROL MASK- sulfer cream
- NDC Code(s): 70809-1906-1
- Packager: USRX LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- 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 irriation occurs, only use one topical acne medication at a time. Avoid contact with eyes. Apply only to areas with acne. Do not use on broken skin or large areas of the skin.
- Directions:
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Inactive ingredients:
WATER, KAOLIN, GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, NIACINAMIDE, GUM ARABIC, CETYL ALCOHOL, BENTONITE, CETEARYL ALCOHOL, CETEARETH-20, BUTYROSPERMUM PARKII (SHEA) BUTTER, SALICYCLIC ACID, HYDROLYZED ARDENIA FLORIDA EXTRACT, MENTHA PIPERITA (PEPPERMINT) OIL, EUCALYPTUS GLOBULUS LEAF OIL, SALIX NIGRA (WILLOW) BARK EXTRACT, TANACETUM ANNUUM, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF JUICE, ALPHA-ARBUTIN, KOJIC ACID, AZELAIC ACID, RETINYL PALMITATE, TOCOPHEROL OIL, VACCINIUM MACOCARPON (CRANBERRY) FRUIT EXTRACT, XANTHAN GUM, MALTODEXTRIN, SODIUM PCA, CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, GLUTATHIONE, TARTARIC ACID, CITRIC ACID, PHENOXYETHANOL, ETHYLHEXAYLGLYCERIN.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE AND BLEMISH CONTROL MASK
sulfer creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70809-1906 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 5 g in 100 mL Inactive Ingredients Ingredient Name Strength SALICYLIC ACID (UNII: O414PZ4LPZ) CETYL ALCOHOL (UNII: 936JST6JCN) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) GARDENIA JASMINOIDES WHOLE (UNII: 0PK353KHF0) ACACIA (UNII: 5C5403N26O) BENTONITE (UNII: A3N5ZCN45C) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CRANBERRY JUICE (UNII: Y74M3X3345) SODIUM PIDOLATE (UNII: 1V74VH163T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) PEPPERMINT OIL (UNII: AV092KU4JH) AZELAIC ACID (UNII: F2VW3D43YT) MALTODEXTRIN (UNII: 7CVR7L4A2D) TARTARIC ACID (UNII: W4888I119H) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUTATHIONE (UNII: GAN16C9B8O) NIACINAMIDE (UNII: 25X51I8RD4) MENTHA PIPERITA (UNII: 79M2M2UDA9) SALIX NIGRA BARK (UNII: QU52J3A5B3) SHEA BUTTER (UNII: K49155WL9Y) TOCOPHEROL (UNII: R0ZB2556P8) GLYCERIN (UNII: PDC6A3C0OX) TANSY OIL (UNII: 43J2812KE1) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) KAOLIN (UNII: 24H4NWX5CO) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALPHA-ARBUTIN (UNII: 72VUP07IT5) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) XANTHAN GUM (UNII: TTV12P4NEE) GREEN TEA LEAF (UNII: W2ZU1RY8B0) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) KOJIC ACID (UNII: 6K23F1TT52) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70809-1906-1 1 in 1 BOX 04/28/2020 1 73.93 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 Drug M006 04/28/2020 Labeler - USRX LLC (115270633) Establishment Name Address ID/FEI Business Operations Packaging On Demand, Inc. 610511326 manufacture(70809-1906)