NDC 15631-0072

BAPTISIA TINCTORIA

Baptisia Tinctoria

BAPTISIA TINCTORIA is a Oral Pellet 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 ID15631-0072_9eca05d1-7b87-24e9-e053-2a95a90ac2f1
NDC15631-0072
Product TypeHuman Otc Drug
Proprietary NameBAPTISIA TINCTORIA
Generic NameBaptisia Tinctoria
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
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 FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0072-0

100 PELLET in 1 PACKAGE (15631-0072-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0072-1 [15631007201]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0072-2 [15631007202]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0072-0 [15631007200]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0072-3 [15631007203]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0072-4 [15631007204]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0072-5 [15631007205]

BAPTISIA TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

Drug Details

Active Ingredients

IngredientStrength
BAPTISIA TINCTORIA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:cdc01e02-8ac4-4b87-97c7-34b35b2f548a
Manufacturer
UNII

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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