- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- cleanse the skin thoroughly before applying
- cover the entire affected area with a thin layer one to three times daily
- leave on for 10 minutes
- thoroughly remove with water
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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
Avena sativa (oat) kernel colloidal oatmeal, bentonite, Butyrospermum parkii (shea) butter, cetearyl glucoside, citric acid, glycerin, glyceryl stearate, Helianthus annuus (sunflower) seed oil, hydrogenated castor oil, phenoxyethanol, potassium sorbate, purified water, sodium stearoyl glutamate, xanthan gum
- Questions
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 27 g Tube Box
-
INGREDIENTS AND APPEARANCE
EARTHS CARE ACNE SPOT TREATMENT
sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1557 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 10 g in 100 g Inactive Ingredients Ingredient Name Strength OATMEAL (UNII: 8PI54V663Y) BENTONITE (UNII: A3N5ZCN45C) SHEA BUTTER (UNII: K49155WL9Y) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SUNFLOWER OIL (UNII: 3W1JG795YI) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24286-1557-1 1 in 1 BOX 01/18/2013 1 27 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:24286-1557-2 2.8 g in 1 POUCH; Type 0: Not a Combination Product 01/18/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/18/2013 Labeler - DLC Laboratories, Inc. (093351930) Establishment Name Address ID/FEI Business Operations DLC Laboratories, Inc. 093351930 manufacture(24286-1557)