KREOSOTUM

Product NDC
15631-2807
Type
HUMAN OTC DRUG
Nonproprietary name
KREOSOTUM
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
WOOD CREOSOTE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
15631-2807-010 mL in 1 BOTTLE (15631-2807-0) 2024-05-23NoHistorical
15631-2807-130 mL in 1 BOTTLE (15631-2807-1) 2024-05-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
KREOSOTUM - Rxhomeo Private Limited d.b.a. Rxhomeo, IncRxhomeo Private Limited d.b.a. Rxhomeo, Inc2024-06-06HUMAN OTC DRUG LABEL1