IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%

Product NDC
72934-1131
Requested package NDC
72934-1131-2
11-digit product format
729341131
Labeler code
72934
Product ID
72934-1131_a7464b24-e0ab-b466-e053-2995a90a997e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%
Dosage form
GEL
Route
TOPICAL
Labeler
Sincerus Florida, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-05-01
Marketing end
0000-00-00
Substance
METRONIDAZOLE; IVERMECTIN; NIACINAMIDE
Active strength
1 g/100g; g/100g; g/100g
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS],Antiparasitic [EPC],Pediculicide [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72934-113172934-1131-2IInactivated by FDA2026-08-03

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8ffb9b1d-3ed7-ba2e-677e-47d4d134fd55Product name520251024
7f6d14e0-4366-41bc-a4a9-b74c79a20e17Product name120250623
7fd951fe-040a-0b64-2bea-eefc6aa4fc54Product name220250515
e6d321b0-0e5e-7da6-f043-92b6a91f00a1Product name520250515
e1aac33b-94ae-4ee9-905b-299f7263853bProduct name320250124
16642716-d28a-4f90-8dcb-3921cd8c8109Product name420240516
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
5b0ed980-56ce-7dd0-fb86-ff54be67c2e6Product name220200925
eed31638-1288-4eb6-a55c-5fc014dca98dProduct name320200728
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
a5070875-62bb-61e1-fd46-8f7054197a40Product name820180215
0add4de9-d152-3375-3390-1123dddc5e3dProduct name120140508
33ca0fcc-1011-92dc-50a9-a383683eed1eProduct name120140508
53f39d9f-cd3f-04e1-c668-d4580719d57dProduct name120140508
a804000f-b74f-0b5d-d17b-aa767c286ddbProduct name120140508
a91ea265-6e02-c08f-93c8-686d54180529Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-1131-22022-01-28C16284748780-1d6a99b39-5a12-a426-e053-dadaa90af4c2IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-1131-2IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%30 g in 1 BOTTLE, PUMPGEL302

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72934-1131-2GM - Gram72934-1131a72384a8-c65e-464f-a9e7-9c0ec98c6c1d12020-02-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-1131IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4% GEL [SINCERUS FLORIDA, LLC]2Legacy NDC, 1 package rows20200605_874c79d7-7768-3d66-e053-2995a90a6d5c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72934-1131-27293411310230 g in 1 BOTTLE, PUMP (72934-1131-2) 30 g2019-05-010000-00-00NoNoCurrent