IVERMECTIN 1% / METRONIDAZOLE 1%
- Product NDC
- 72934-1130
- 11-digit product format
- 729341130
- Labeler code
- 72934
- Product ID
- 72934-1130_874c79d7-7767-3d66-e053-2995a90a6d5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- IVERMECTIN 1% / METRONIDAZOLE 1%
- 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
- Active strength
- 1 g/100g; g/100g
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS],Antiparasitic [EPC],Pediculicide [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 72934-1130 | I | Inactivated by FDA | 2026-08-03 | ||
| excluded package | package | 72934-1130 | 72934-1130-2 | I | Inactivated by FDA | 2026-08-03 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 8ffb9b1d-3ed7-ba2e-677e-47d4d134fd55 | Product name | 5 | 20251024 |
| 7f6d14e0-4366-41bc-a4a9-b74c79a20e17 | Product name | 1 | 20250623 |
| 7fd951fe-040a-0b64-2bea-eefc6aa4fc54 | Product name | 2 | 20250515 |
| e6d321b0-0e5e-7da6-f043-92b6a91f00a1 | Product name | 5 | 20250515 |
| e1aac33b-94ae-4ee9-905b-299f7263853b | Product name | 3 | 20250124 |
| 16642716-d28a-4f90-8dcb-3921cd8c8109 | Product name | 4 | 20240516 |
| 0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15 | Product name | 1 | 20240313 |
| 5b0ed980-56ce-7dd0-fb86-ff54be67c2e6 | Product name | 2 | 20200925 |
| eed31638-1288-4eb6-a55c-5fc014dca98d | Product name | 3 | 20200728 |
| dea2eded-d1e7-46bb-9a3d-f8dc20de6277 | Product name | 1 | 20190408 |
| a5070875-62bb-61e1-fd46-8f7054197a40 | Product name | 8 | 20180215 |
| 0add4de9-d152-3375-3390-1123dddc5e3d | Product name | 1 | 20140508 |
| 33ca0fcc-1011-92dc-50a9-a383683eed1e | Product name | 1 | 20140508 |
| 53f39d9f-cd3f-04e1-c668-d4580719d57d | Product name | 1 | 20140508 |
| a804000f-b74f-0b5d-d17b-aa767c286ddb | Product name | 1 | 20140508 |
| a91ea265-6e02-c08f-93c8-686d54180529 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72934-1130-2 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2641-a910-e053-dadaa90a0b85 | IVERMECTIN 1% / METRONIDAZOLE 1% |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72934-1130-2 | IVERMECTIN 1% / METRONIDAZOLE 1% | 30 g in 1 BOTTLE, PUMP | GEL | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72934-1130 | IVERMECTIN 1% / METRONIDAZOLE 1% GEL [SINCERUS FLORIDA, LLC] | 1 | Legacy NDC, 1 package rows | 20190501_874c79d7-7766-3d66-e053-2995a90a6d5c.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 72934-1130-2 | 72934113002 | 30 g in 1 BOTTLE, PUMP | 30 g | Historical |