NDC 15631-0256

KREOSOTUM

Kreosotum

KREOSOTUM 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 Wood Creosote.

Product ID15631-0256_126d7672-3154-408e-b4e9-860b0ab7ad08
NDC15631-0256
Product TypeHuman Otc Drug
Proprietary NameKREOSOTUM
Generic NameKreosotum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameWOOD CREOSOTE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0256-0

100 PELLET in 1 PACKAGE (15631-0256-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0256-1 [15631025601]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0256-5 [15631025605]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0256-0 [15631025600]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0256-3 [15631025603]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0256-2 [15631025602]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0256-4 [15631025604]

KREOSOTUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
WOOD CREOSOTE3 [hp_X]/1

OpenFDA Data

SPL SET ID:3d11b6a2-8f58-4db1-a1f3-9f810b3b5826
Manufacturer
UNII

NDC Crossover Matching brand name "KREOSOTUM" or generic name "Kreosotum"

NDCBrand NameGeneric Name
0220-2940KreosotumWOOD CREOSOTE
0220-2943KreosotumWOOD CREOSOTE
0220-2944KreosotumWOOD CREOSOTE
0220-2946KreosotumWOOD CREOSOTE
15631-0256KREOSOTUMKREOSOTUM
15631-0615KREOSOTUMKREOSOTUM
68428-461KreosotumWOOD CREOSOTE
71919-394KreosotumWOOD CREOSOTE
69152-1048Kreosotum 200CKreosotum

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