NDC 15631-0036

ANTIMONIUM CRUDUM

Antimonium Crudum

ANTIMONIUM CRUDUM 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 Antimony Trisulfide.

Product ID15631-0036_9e3927bf-1ba6-13cb-e053-2995a90af8bd
NDC15631-0036
Product TypeHuman Otc Drug
Proprietary NameANTIMONIUM CRUDUM
Generic NameAntimonium Crudum
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 NameANTIMONY TRISULFIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0036-0

100 PELLET in 1 PACKAGE (15631-0036-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0036-2 [15631003602]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0036-4 [15631003604]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0036-1 [15631003601]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0036-3 [15631003603]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0036-5 [15631003605]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0036-0 [15631003600]

ANTIMONIUM CRUDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
ANTIMONY TRISULFIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:7e9b478f-1eab-4473-8138-3680dcaa4bfc
Manufacturer
UNII

NDC Crossover Matching brand name "ANTIMONIUM CRUDUM" or generic name "Antimonium Crudum"

NDCBrand NameGeneric Name
0220-0345Antimonium crudumANTIMONY TRISULFIDE
0220-0346Antimonium crudumANTIMONY TRISULFIDE
0220-0349Antimonium crudumANTIMONY TRISULFIDE
0220-0350Antimonium crudumANTIMONY TRISULFIDE
0220-0353Antimonium crudumANTIMONY TRISULFIDE
0220-0354Antimonium crudumANTIMONY TRISULFIDE
0220-0357Antimonium crudumANTIMONY TRISULFIDE
0220-0358Antimonium crudumANTIMONY TRISULFIDE
0220-0369Antimonium crudumANTIMONY TRISULFIDE
0220-0372Antimonium crudumANTIMONY TRISULFIDE
15631-0036ANTIMONIUM CRUDUMANTIMONIUM CRUDUM
15631-0513ANTIMONIUM CRUDUMANTIMONIUM CRUDUM
53645-1120Antimonium CrudumAntimonium Crudum
60512-1003ANTIMONIUM CRUDUMANTIMONIUM CRUDUM
62106-4852ANTIMONIUM CRUDUMAntimony trisulfide
63545-010Antimonium CrudumAnitmonium Crudum
63545-011Antimonium CrudumAnitmonium Crudum
63545-012Antimonium CrudumAnitmonium Crudum
63545-013Antimonium CrudumAnitmonium Crudum
63545-014Antimonium CrudumAnitmonium Crudum
63545-015Antimonium CrudumAnitmonium Crudum
63545-016Antimonium CrudumAnitmonium Crudum
63545-017Antimonium CrudumAnitmonium Crudum
63545-018Antimonium CrudumAnitmonium Crudum
68428-212Antimonium crudumANTIMONY TRISULFIDE
71919-064Antimonium crudumANTIMONY TRISULFIDE
79718-1073Antimonium CrudumAntimonium Crudum
69152-1031Antimonium crudum 200CAntimonium crudum
69152-1175Antimonium crudum 6CAntimonium crudum

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