KREOSOTUM

Product NDC
15631-0615
11-digit product format
156310615
Labeler code
15631
Product ID
15631-0615_1e087225-bccf-4295-aaaf-f9e699cb962e
Type
HUMAN OTC DRUG
Nonproprietary name
KREOSOTUM
Dosage form
TABLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-12-18
Marketing end
0000-00-00
Substance
WOOD CREOSOTE
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0615-0KREOSOTUM1 in 1 BLISTER PACKTABLET11
15631-0615-1KREOSOTUM4 in 1 BLISTER PACKTABLET41
15631-0615-2KREOSOTUM50 in 1 CONTAINERTABLET501
15631-0615-3KREOSOTUM100 in 1 CONTAINERTABLET1001
15631-0615-4KREOSOTUM250 in 1 CONTAINERTABLET2501
15631-0615-5KREOSOTUM500 in 1 CONTAINERTABLET5001
15631-0615-6KREOSOTUM1000 in 1 CONTAINERTABLET10001
15631-0615-7KREOSOTUM10000 in 1 CONTAINERTABLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0615KREOSOTUM TABLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Legacy NDC, 8 package rows20151230_adc9b980-01d8-4c9e-ac91-b0646b101618.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
15631-0615-0156310615001 in 1 BLISTER PACKHistorical
15631-0615-1156310615014 in 1 BLISTER PACKHistorical
15631-0615-21563106150250 in 1 CONTAINERHistorical
15631-0615-315631061503100 in 1 CONTAINERHistorical
15631-0615-415631061504250 in 1 CONTAINERHistorical
15631-0615-515631061505500 in 1 CONTAINERHistorical
15631-0615-6156310615061000 in 1 CONTAINERHistorical
15631-0615-71563106150710000 in 1 CONTAINERHistorical