Label: SYZYGIUM JAMBOLANUM 1X- syzygium jambolanum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69152-1553-1 - Packager: Paramesh Banerji Life Sciences LLC
- Category: HUMAN PRESCRIPTION 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 June 5, 2015
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- Official Label (Printer Friendly)
- Active Ingredients
- Inactive Ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children
- Direction
- Manufactured by
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SYZYGIUM JAMBOLANUM 1X
syzygium jambolanum liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69152-1553 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (SYZYGIUM CUMINI SEED - UNII:820LSF646I) SYZYGIUM CUMINI SEED 1 [hp_X] in 8 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Product Characteristics Color brown (Reddish Brown) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69152-1553-1 8 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 06/05/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/05/2015 Labeler - Paramesh Banerji Life Sciences LLC (079393726) Establishment Name Address ID/FEI Business Operations Paramesh Banerji Life Sciences LLC 079393726 manufacture(69152-1553) , pack(69152-1553) , label(69152-1553)
