NDC 15631-0217

HEDEOMA PULEGIOIDES

Hedeoma Pulegioides

HEDEOMA PULEGIOIDES 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 Hedeoma Pulegioides.

Product ID15631-0217_9ae2f232-556c-4e07-aea1-08357099293c
NDC15631-0217
Product TypeHuman Otc Drug
Proprietary NameHEDEOMA PULEGIOIDES
Generic NameHedeoma Pulegioides
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameHEDEOMA PULEGIOIDES
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0217-0

100 PELLET in 1 PACKAGE (15631-0217-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0217-1 [15631021701]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0217-0 [15631021700]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0217-3 [15631021703]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0217-4 [15631021704]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0217-5 [15631021705]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0217-2 [15631021702]

HEDEOMA PULEGIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
HEDEOMA PULEGIOIDES3 [hp_X]/1

OpenFDA Data

SPL SET ID:f8b686a4-fb58-4c89-a7de-faaf6eae9fca
Manufacturer
UNII

NDC Crossover Matching brand name "HEDEOMA PULEGIOIDES" or generic name "Hedeoma Pulegioides"

NDCBrand NameGeneric Name
15631-0217HEDEOMA PULEGIOIDESHEDEOMA PULEGIOIDES
68428-419Hedeoma pulegioidesHEDEOMA PULEGIOIDES
71919-333Hedeoma pulegioidesHEDEOMA PULEGIOIDES

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