NDC 15631-0470

ZINCUM MURIATICUM

Zincum Muriaticum

ZINCUM MURIATICUM 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 Zinc Chloride.

Product ID15631-0470_980ea854-4615-414a-aaa9-a8414ed54d49
NDC15631-0470
Product TypeHuman Otc Drug
Proprietary NameZINCUM MURIATICUM
Generic NameZincum Muriaticum
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 NameZINC CHLORIDE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0470-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0470-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0470-1 [15631047001]

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

NDC 15631-0470-4 [15631047004]

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

NDC 15631-0470-0 [15631047000]

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

NDC 15631-0470-2 [15631047002]

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

NDC 15631-0470-3 [15631047003]

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

NDC 15631-0470-5 [15631047005]

ZINCUM MURIATICUM 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
ZINC CHLORIDE6 [hp_X]/1

OpenFDA Data

SPL SET ID:0bf6630c-a578-499c-a8c9-9c5f5da03114
Manufacturer
UNII

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