Label: SYMPHYTUM OFFICINALE 7139- symphytum officinale liquid
- NDC Code(s): 63083-7139-1
- Packager: Professional Complementary Health Formulas
- Category: HUMAN OTC DRUG LABEL
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.
Updated August 15, 2019
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- ACTIVE INGREDIENTS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
INGREDIENTS AND APPEARANCE
SYMPHYTUM OFFICINALE 7139
symphytum officinale liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-7139 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 6 [hp_X] in 29.5 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-7139-1 29.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-7139)