NDC 15631-0300

MURIATICUM ACIDUM

Muriaticum Acidum

MURIATICUM 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 Hydrochloric Acid.

Product ID15631-0300_3f67d7e0-13f3-41e2-b2b1-ba0779aeff0d
NDC15631-0300
Product TypeHuman Otc Drug
Proprietary NameMURIATICUM ACIDUM
Generic NameMuriaticum Acidum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameHYDROCHLORIC ACID
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0300-0

100 PELLET in 1 PACKAGE (15631-0300-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0300-0 [15631030000]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0300-5 [15631030005]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0300-3 [15631030003]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0300-1 [15631030001]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0300-4 [15631030004]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0300-2 [15631030002]

MURIATICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLORIC ACID6 [hp_X]/1

OpenFDA Data

SPL SET ID:bf918100-6bf0-42f2-8332-29b116ed2770
Manufacturer
UNII

NDC Crossover Matching brand name "MURIATICUM ACIDUM" or generic name "Muriaticum Acidum"

NDCBrand NameGeneric Name
0220-3466Muriaticum acidumHYDROCHLORIC ACID
0220-3467Muriaticum acidumHYDROCHLORIC ACID
0220-3473Muriaticum acidumHYDROCHLORIC ACID
0220-3474Muriaticum acidumHYDROCHLORIC ACID
0220-3475Muriaticum acidumHYDROCHLORIC ACID
15631-0300MURIATICUM ACIDUMMURIATICUM ACIDUM
68428-516Muriaticum acidumHYDROCHLORIC ACID
71919-471Muriaticum acidumHYDROCHLORIC ACID

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