Label: NAT SULPH 3X- natrum sulph 3x tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 79718-5051-1 - Packager: Warsan Homeopathic
- This is a repackaged label.
- Source NDC Code(s): 79769-0051
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated October 27, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- PURPOSE
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DOSAGE & ADMINISTRATION
Adults and children 12 years of age and older: Four tablets every thirty minutes for six doses followed by four tablets every 4-6 hours as needed.
Children 2 years to 12 years of age: Four tablets every thirty minutes for six doses followed by two tablets every 4-6 hours as needed.
Children under 2 years of age: Consult doctor prior to use.
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NAT SULPH 3X
natrum sulph 3x tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79718-5051(NDC:79769-0051) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM SULFATE ANHYDROUS 3 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color white Score no score Shape ROUND Size 6mm Flavor Imprint Code SBL Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79718-5051-1 900 in 1 JAR; Type 0: Not a Combination Product 12/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/07/2020 Labeler - Warsan Homeopathic (081031642)
