Label: NATRUM SULPHURICUM- sodium sulfate tablet, chewable
- NDC Code(s): 60512-8032-5, 60512-8032-6
- Packager: HOMEOLAB USA INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
Updated March 25, 2014
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- Active ingredients HPUS
Natrum sulphuricum (Sodium sulphate) 12XClose
...........................................Nausea, vomiting, flatulent diarrheaClose
The letters 'HPUS' indicate that the component in this product is officially monographed in the Homoeopathic Pharmacopoeia of the United States.Close
This tissue salt helps relieve symptoms of nausea, vomiting and flatulent diarrhea.*
*These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.Close
Keep this and all medications out of the reach of children.
In case of emergency or accidental overdose, contact a medical professional or a Poison Control Center immediately.
Children from 2 to 5 years: Crush 2 tablets and dissolve in water 3 times daily, or as directed by a healthcare professional.
Adults and children over 5 years: Chew 2 tablets 3 times daily, or as directed by a healthcare professional.
• Do not use more than directed.
• Do not take with food.Close
- Other information
Store at room temperature.
Do not use if cap seal is broken or missing.Close
- Inactive ingredients
Lactose, magnesium stearate.Close
- INGREDIENTS AND APPEARANCE
natrum sulphuricum tablet, chewable
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-8032 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 12 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score no score Shape ROUND Size 8mm Flavor Imprint Code NONE Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60512-8032-5 125 in 1 JAR 2 NDC:60512-8032-6 500 in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/25/2014 Labeler - HOMEOLAB USA INC (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC 202032533 manufacture(60512-8032)