NDC 15631-0440

THIOSINAMINUM

Thiosinaminum

THIOSINAMINUM 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 Allylthiourea.

Product ID15631-0440_a1d0cde9-34a8-94ce-e053-2a95a90afa81
NDC15631-0440
Product TypeHuman Otc Drug
Proprietary NameTHIOSINAMINUM
Generic NameThiosinaminum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameALLYLTHIOUREA
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0440-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0440-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0440-5 [15631044005]

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

NDC 15631-0440-0 [15631044000]

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

NDC 15631-0440-4 [15631044004]

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

NDC 15631-0440-2 [15631044002]

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

NDC 15631-0440-3 [15631044003]

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

NDC 15631-0440-1 [15631044001]

THIOSINAMINUM 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
ALLYLTHIOUREA3 [hp_X]/1

OpenFDA Data

SPL SET ID:44c6781e-625f-4ae1-8475-c8bef6ccc62e
Manufacturer
UNII

NDC Crossover Matching brand name "THIOSINAMINUM" or generic name "Thiosinaminum"

NDCBrand NameGeneric Name
0220-4971ThiosinaminumALLYLTHIOUREA
0220-4972ThiosinaminumALLYLTHIOUREA
0220-4979ThiosinaminumALLYLTHIOUREA
0220-4980ThiosinaminumALLYLTHIOUREA
0220-4983ThiosinaminumALLYLTHIOUREA
0220-4984ThiosinaminumALLYLTHIOUREA
15631-0440THIOSINAMINUMTHIOSINAMINUM
15631-0698THIOSINAMINUMTHIOSINAMINUM
15631-2323THIOSINAMINUMTHIOSINAMINUM
37662-2305ThiosinaminumThiosinaminum
37662-2306ThiosinaminumThiosinaminum
37662-2307ThiosinaminumThiosinaminum
37662-2308ThiosinaminumThiosinaminum
37662-2309ThiosinaminumThiosinaminum
37662-2310ThiosinaminumThiosinaminum
37662-2311ThiosinaminumThiosinaminum
37662-2312ThiosinaminumThiosinaminum
62106-6482THIOSINAMINUMThiosinamine
68428-674ThiosinaminumALLYLTHIOUREA
71919-675THIOSINAMINUMAllylthiourea
68428-721Be gone ScarsTHIOSINAMINUM

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