NDC 15631-0533

BAPTISIA TINCTORIA

Baptisia Tinctoria

BAPTISIA TINCTORIA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Baptisia Tinctoria Root.

Product ID15631-0533_6bb04ecf-f1f7-4379-bc55-1eb0beb4380b
NDC15631-0533
Product TypeHuman Otc Drug
Proprietary NameBAPTISIA TINCTORIA
Generic NameBaptisia Tinctoria
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameBAPTISIA TINCTORIA ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0533-5

500 TABLET in 1 CONTAINER (15631-0533-5)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0533-6 [15631053306]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-2 [15631053302]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-7 [15631053307]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-1 [15631053301]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-4 [15631053304]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-5 [15631053305]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-0 [15631053300]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0533-3 [15631053303]

BAPTISIA TINCTORIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:b7974277-d734-4391-9d2f-494530c29d43
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "BAPTISIA TINCTORIA" or generic name "Baptisia Tinctoria"

    NDCBrand NameGeneric Name
    0220-0770Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    0220-0773Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    0220-0774Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    0220-0775Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    15631-0072BAPTISIA TINCTORIABAPTISIA TINCTORIA
    15631-0533BAPTISIA TINCTORIABAPTISIA TINCTORIA
    53645-1920Baptisia TinctoriaBaptisia Tinctoria
    60512-6537BAPTISIA TINCTORIABAPTISIA TINCTORIA
    63083-7105Baptisia tinctoriaBaptisia tinctoria
    63545-352Baptisia TinctoriaBaptisia Tinctoria
    63545-353Baptisia TinctoriaBaptisia Tinctoria
    63545-354Baptisia TinctoriaBaptisia Tinctoria
    63545-355Baptisia TinctoriaBaptisia Tinctoria
    63545-356Baptisia TinctoriaBaptisia Tinctoria
    63545-357Baptisia TinctoriaBaptisia Tinctoria
    63545-358Baptisia TinctoriaBaptisia Tinctoria
    63545-359Baptisia TinctoriaBaptisia Tinctoria
    66096-794Baptisia TinctoriaBAPTISIA TINCTORIA
    68428-247Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    71919-109Baptisia tinctoriaBAPTISIA TINCTORIA ROOT
    69152-1560Baptisia tinctoria 1XBaptisia tinctoria
    69152-1089Baptisia tinctoria 200CBaptisia tinctoria
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