Nicotine Mini
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Nicotine Mini
- Generic name
- NICOTINE POLACRILEX
- Manufacturer
- Advagen Pharma Limited
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7f124912-7ce8-4b9f-8458-46b68362f47d
- SPL ID
- 4859954c-e904-be9f-e063-6294a90a1804
- Version
- 2
- Effective date
- 2026-01-14
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:49
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 208875 | derived:openfda.application_number |
| application number | ANDA208875 | openfda.application_number | |
| brand name | Nicotine Mini | openfda.brand_name | |
| generic name | NICOTINE POLACRILEX | openfda.generic_name | |
| manufacturer name | Advagen Pharma Limited | openfda.manufacturer_name | |
| ndc | package | 72888-187-56 | openfda.package_ndc |
| ndc | package | 72888-186-56 | openfda.package_ndc |
| ndc | package | 72888-187-53 | openfda.package_ndc |
| ndc | package | 72888-186-55 | openfda.package_ndc |
| ndc | package | 72888-187-55 | openfda.package_ndc |
| ndc | package | 72888-187-54 | openfda.package_ndc |
| ndc | package | 72888-186-54 | openfda.package_ndc |
| ndc | package | 72888-186-53 | openfda.package_ndc |
| ndc | product | 72888-187 | openfda.product_ndc |
| ndc | product | 72888-186 | openfda.product_ndc |
| ndc11 | package | 72888018653 | derived:openfda.package_ndc |
| ndc11 | package | 72888018756 | derived:openfda.package_ndc |
| ndc11 | package | 72888018654 | derived:openfda.package_ndc |
| ndc11 | package | 72888018754 | derived:openfda.package_ndc |
| ndc11 | package | 72888018655 | derived:openfda.package_ndc |
| ndc11 | package | 72888018656 | derived:openfda.package_ndc |
| ndc11 | package | 72888018753 | derived:openfda.package_ndc |
| ndc11 | package | 72888018755 | derived:openfda.package_ndc |
| rxcui | 359817 | openfda.rxcui | |
| rxcui | 359818 | openfda.rxcui | |
| spl id | 4859954c-e904-be9f-e063-6294a90a1804 | id | |
| spl set id | 7f124912-7ce8-4b9f-8458-46b68362f47d | set_id | |
| unii | 6M3C89ZY6R | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.