NDC 15631-0025

AMMONIUM BENZOICUM

Ammonium Benzoicum

AMMONIUM BENZOICUM 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 Ammonium Benzoate.

Product ID15631-0025_9e4a93d1-5a93-2445-e053-2995a90a770b
NDC15631-0025
Product TypeHuman Otc Drug
Proprietary NameAMMONIUM BENZOICUM
Generic NameAmmonium Benzoicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAMMONIUM BENZOATE
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0025-0

100 PELLET in 1 PACKAGE (15631-0025-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0025-0 [15631002500]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0025-1 [15631002501]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0025-4 [15631002504]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0025-2 [15631002502]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0025-3 [15631002503]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0025-5 [15631002505]

AMMONIUM BENZOICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM BENZOATE2 [hp_X]/1

OpenFDA Data

SPL SET ID:e5fe6e55-a1da-4b80-b07f-7e3415e0288b
Manufacturer
UNII

NDC Crossover Matching brand name "AMMONIUM BENZOICUM" or generic name "Ammonium Benzoicum"

NDCBrand NameGeneric Name
15631-0025AMMONIUM BENZOICUMAMMONIUM BENZOICUM
68428-876Ammonium benzoicumAMMONIUM BENZOATE
71919-040Ammonium benzoicumAMMONIUM BENZOATE

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