Label: SPOT CORRECTION- sulfur cream
- NDC Code(s): 60934-002-01
- Packager: HydroPeptide LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 9, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
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Warnings
For external use only
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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
- Other Information
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Inactive Ingredients
4-t-Butylcyclohexanol, Acacia Senegal Gum, Arginine, Chondrus Crispus (Carrageenan), Citrus Grandis (Grapefruit) Peel Oil, Epilobium Angustifolium Flower/Leaf/Stem Extract, Lactic Acid, Leuconostoc/Radish Root Ferment Filtrate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Niacinamide, Pentylene Glycol, Rice Ferment (Sake) Filtrate, Sodium Hydroxide, Water (Aqua), Xanthan Gum
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
SPOT CORRECTION
sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60934-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength 4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C) ACACIA (UNII: 5C5403N26O) ARGININE (UNII: 94ZLA3W45F) CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78) CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44) EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D) LACTIC ACID (UNII: 33X04XA5AT) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) TEA TREE OIL (UNII: VIF565UC2G) NIACINAMIDE (UNII: 25X51I8RD4) PENTYLENE GLYCOL (UNII: 50C1307PZG) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60934-002-01 1 in 1 BOX 01/11/2017 1 15 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 01/11/2017 Labeler - HydroPeptide LLC (006297465)