NDC 15631-0615

KREOSOTUM

Kreosotum

KREOSOTUM is a Oral Tablet 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 ID15631-0615_1e087225-bccf-4295-aaaf-f9e699cb962e
NDC15631-0615
Product TypeHuman Otc Drug
Proprietary NameKREOSOTUM
Generic NameKreosotum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-18
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 15631-0615-0

1 TABLET in 1 BLISTER PACK (15631-0615-0)
Marketing Start Date2015-12-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0615-2 [15631061502]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-1 [15631061501]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-3 [15631061503]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-7 [15631061507]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-4 [15631061504]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-0 [15631061500]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-5 [15631061505]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

NDC 15631-0615-6 [15631061506]

KREOSOTUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
WOOD CREOSOTE3 [hp_X]/1

OpenFDA Data

SPL SET ID:adc9b980-01d8-4c9e-ac91-b0646b101618
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.