NDC 15631-0078

BENZOICUM ACIDUM

Benzoicum Acidum

BENZOICUM ACIDUM 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 Benzoic Acid.

Product ID15631-0078_79975c51-bdba-4935-a4de-1ff447cf90ee
NDC15631-0078
Product TypeHuman Otc Drug
Proprietary NameBENZOICUM ACIDUM
Generic NameBenzoicum Acidum
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 NameBENZOIC ACID
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0078-0

100 PELLET in 1 PACKAGE (15631-0078-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0078-3 [15631007803]

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

NDC 15631-0078-5 [15631007805]

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

NDC 15631-0078-0 [15631007800]

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

NDC 15631-0078-2 [15631007802]

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

NDC 15631-0078-1 [15631007801]

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

NDC 15631-0078-4 [15631007804]

BENZOICUM ACIDUM 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
BENZOIC ACID1 [hp_X]/1

OpenFDA Data

SPL SET ID:0fb9916c-7052-4dee-9c33-5f4f69c2cd23
Manufacturer
UNII

NDC Crossover Matching brand name "BENZOICUM ACIDUM" or generic name "Benzoicum Acidum"

NDCBrand NameGeneric Name
0220-0823Benzoicum acidumBENZOIC ACID
0220-0824Benzoicum acidumBENZOIC ACID
15631-0078BENZOICUM ACIDUMBENZOICUM ACIDUM
60512-6203BENZOICUM ACIDUMBENZOICUM ACIDUM
66096-799Benzoicum AcidumBENZOICUM ACIDUM
71919-117Benzoicum acidumBENZOIC ACID

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