NDC 15631-0473

ZINGIBER OFFICINALE

Zingiber Officinale

ZINGIBER OFFICINALE 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 Ginger.

Product ID15631-0473_a1d477d0-c097-413c-e053-2995a90aea64
NDC15631-0473
Product TypeHuman Otc Drug
Proprietary NameZINGIBER OFFICINALE
Generic NameZingiber Officinale
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGINGER
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0473-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0473-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0473-0 [15631047300]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0473-2 [15631047302]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0473-3 [15631047303]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0473-1 [15631047301]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0473-5 [15631047305]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0473-4 [15631047304]

ZINGIBER OFFICINALE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
GINGER1 [hp_X]/1

OpenFDA Data

SPL SET ID:bb53274a-bd94-436d-a0b2-15860c8aa6bc
Manufacturer
UNII

NDC Crossover Matching brand name "ZINGIBER OFFICINALE" or generic name "Zingiber Officinale"

NDCBrand NameGeneric Name
15631-0473ZINGIBER OFFICINALEZINGIBER OFFICINALE
15631-0708ZINGIBER OFFICINALEZINGIBER OFFICINALE
68428-717Zingiber officinaleGINGER
22840-5723GingerZingiber officinale
71919-734ZINGIBERZINGIBER OFFICINALE

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.