NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025%
- Manufacturer
- Sincerus Florida, LLC
- Effective date
- 2019-05-03
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 20:28:34
Label at a glance#
ProductNIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025%
Active ingredientNIACINAMIDE, SPIRONOLACTONE, TRETINOIN
Label structure4 sections
Label contents#
Full prescribing information#
Sincerus Florida, LLC adverse reactions
Actives, inactives
NDC 72934-1152-2. NIACINAMIDE USP 2% / SPIRONOLACTONE USP 5% / TRETINOIN USP 0.025%. Gel30gm.
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| SPIRONOLACTONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| TRETINOIN Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| b80ad7bc-1b6f-7ef4-1ed0-86cd9f459d60 | Product name | 6 | 20251124 |
| d335cba1-5b36-51c8-120a-594ec9d05330 | Product name | 5 | 20251114 |
| 1426d8f8-b7d5-4053-8554-613df00c0d86 | Product name | 2 | 20250616 |
| 25f5e2cf-3572-477b-994c-aa692751e5a8 | Product name | 2 | 20250616 |
| 0e7b8bf1-c46c-4de6-b26a-0c50e34364ec | Product name | 2 | 20250521 |
| e3af9708-3004-7392-4046-5311eaa8bab5 | Product name | 3 | 20221128 |
| 13e7e7e3-e885-4c79-af6d-dad1aedbb06e | Product name | 1 | 20220128 |
| 503b047e-e62d-4745-9011-522b13bc701b | Product name | 1 | 20181206 |
| 7d41caa2-0b5d-9b03-ab8d-84271de26ef4 | Product name | 2 | 20170314 |
| 50ca9ff5-82dd-9971-4f2c-5845a76a8572 | Product name | 2 | 20150818 |
| 0a8118e4-08c6-b395-9ddc-d3e425e0493a | Product name | 1 | 20140508 |
| 233bcb0a-cf40-b0a1-b346-c83ac2f43579 | Product name | 1 | 20140508 |
| 85490a6b-2306-6bf2-c51b-eb63537dc2da | Product name | 1 | 20140508 |
| f151007d-265d-9fbe-857d-1d44f1cb76ba | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72934-1152-2 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-361e-a910-e053-dadaa90a0b85 | NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025% |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72934-1152-2 | NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025% | 30 g in 1 BOTTLE, PUMP | GEL | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72934-1152 | NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025% GEL [SINCERUS FLORIDA, LLC] | 1 | Legacy NDC, 1 package rows | 20190504_87fef62f-e3c1-a78a-e053-2995a90a96ca.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72934-1152-2 | GM - Gram | 72934-1152 | fb2a7e1e-6098-4985-9002-c503f7f4fef3 | 1 | 2020-02-13 |
Products#
Every source-derived product name is available through these pages.
- NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025%
- NIACINAMIDE
- SPIRONOLACTONE
- TRETINOIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72934-1152 | 72934-1152-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NIACINAMIDE | 25X51I8RD4 | ACTIB |
| SPIRONOLACTONE | 27O7W4T232 | ACTIB |
| TRETINOIN | 5688UTC01R | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 87fef62f-e3c2-a78a-e053-2995a90a96ca | 87fef62f-e3c1-a78a-e053-2995a90a96ca | 2019-05-03 | Adverse reactions | 87fef62f-e3c2-a78a-e053-2995a90a96ca 87fef62f-e3c1-a78a-e053-2995a90a96ca |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


