Label: BAPTISIA TINCTORIA 1X- baptisia tinctoria liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69152-1560-1 - Packager: Paramesh Banerji Life Sciences LLC
- 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 August 25, 2015
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- Official Label (Printer Friendly)
- Active Ingredient
- Inactive Ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children
- Direction
- Manufactured by
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BAPTISIA TINCTORIA 1X
baptisia tinctoria liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69152-1560 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 1 [hp_X] in 8 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Product Characteristics Color brown (Orange-brown to Reddish-brown) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69152-1560-1 8 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/09/2015 Labeler - Paramesh Banerji Life Sciences LLC (079393726) Establishment Name Address ID/FEI Business Operations Paramesh Banerji Life Sciences LLC 079393726 manufacture(69152-1560) , pack(69152-1560) , label(69152-1560)
