Label: SPONGATOS- aconitum napellus - ipecac - calcium sulfide - spongia officinalis liquid
- NDC Code(s): 68428-001-06
- Packager: Washington Homeopathic Products
- 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 December 23, 2019
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- ACTIVE INGREDIENTS
- USES
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- INDICATIONS
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- DIRECTIONS
- INACTIVE INGREDIENTS
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INGREDIENTS AND APPEARANCE
SPONGATOS
aconitum napellus - ipecac - calcium sulfide - spongia officinalis liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 3 [hp_X] in 118 mL IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC 4 [hp_X] in 118 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 118 mL SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68428-001-06 118 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/07/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/07/2010 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(68428-001)