Label: NATURASIL INTERNAL PARASITES- sulfur liquid
- NDC Code(s): 10893-270-30
- Packager: Nature's Innovation, Inc.
- 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 January 14, 2021
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- ACTIVE INGREDIENT
- DESCRIPTION
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NATURASIL INTERNAL PARASITES
sulfur liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10893-270 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength BLACK WALNUT (UNII: 02WM57RXZJ) ALCOHOL (UNII: 3K9958V90M) CLOVE (UNII: K48IKT5321) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10893-270-30 30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2012 Labeler - Nature's Innovation, Inc. (602969854) Establishment Name Address ID/FEI Business Operations Nature's Innovation, Inc. 602969854 manufacture(10893-270)