NDC 15631-0708

ZINGIBER OFFICINALE

Zingiber Officinale

ZINGIBER OFFICINALE 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 Ginger.

Product ID15631-0708_d7e2d456-5421-460d-bb04-1f655323b0f3
NDC15631-0708
Product TypeHuman Otc Drug
Proprietary NameZINGIBER OFFICINALE
Generic NameZingiber Officinale
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGINGER
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0708-7

10000 TABLET in 1 CONTAINER (15631-0708-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0708-2 [15631070802]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-4 [15631070804]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-3 [15631070803]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-7 [15631070807]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-1 [15631070801]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-5 [15631070805]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-0 [15631070800]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0708-6 [15631070806]

ZINGIBER OFFICINALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
GINGER1 [hp_X]/1

OpenFDA Data

SPL SET ID:b4315d18-f37f-4393-98cb-a877264847c5
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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

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