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Drug Facts
Active ingredient
Sulphur 12X HPUS*
* The letters ‘HPUS’ indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United StatesStop use and ask a doctor if
- condition worsens
- symptoms last more than 7 days or clear up and occur again within a few days
Keep out of reach of children.
- If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- adults and children 6 months of age and older
• squeeze wash onto wet hands and work into a rich, creamy lather
• wash face and body, then rinse - for babies under 6 months, consult a doctor
Inactive Ingredients
allantoin, ammonium laureth sulfate, Chinese rhubarb (Rheum palmatum) root extract, citric acid, common purslane (Portulaca oleracea) extract, decyl glucoside, disodium laureth sulfosuccinate, glycerin, PEG-150 distearate, pentadecalactone, polyquaternium-10, sodium benzoate, sodium cocoamphoacetate, soapberry (Sapindus mukurossi) fruit extract, water
- SPL UNCLASSIFIED SECTION
- Carton label
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INGREDIENTS AND APPEARANCE
CALM ECZEMA THERAPY WASH
sulphur 12x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50718-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) GLYCERIN (UNII: PDC6A3C0OX) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PENTADECALACTONE (UNII: OK17S3S98K) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) WATER (UNII: 059QF0KO0R) RHEUM PALMATUM ROOT (UNII: G025DAL7CE) SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y) PURSLANE (UNII: M6S840WXG5) AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50718-0012-1 1 in 1 CARTON 01/01/2018 1 200 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 unapproved homeopathic 01/01/2018 Labeler - Kamedis (080311300) Establishment Name Address ID/FEI Business Operations Biogenesis Inc. 069117328 manufacture(50718-0012)