warnings
Warnings for this product
Antispetic
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
- Antispetic
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- Old East Main Co.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1cfd85f3-ef19-46f6-8225-287a8a0a32fd
- SPL ID
- 4c0ff1c3-8a5e-67fd-e063-6394a90ad653
- Version
- 22
- Effective date
- 2026-03-02
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:15
| 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 number | M505G(a)(3) | openfda.application_number | |
| brand name | Antispetic | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Old East Main Co. | openfda.manufacturer_name | |
| ndc | package | 55910-664-12 | openfda.package_ndc |
| ndc | package | 55910-664-77 | openfda.package_ndc |
| ndc | package | 55910-664-19 | openfda.package_ndc |
| ndc | package | 55910-664-69 | openfda.package_ndc |
| ndc | product | 55910-664 | openfda.product_ndc |
| ndc11 | package | 55910066412 | derived:openfda.package_ndc |
| ndc11 | package | 55910066477 | derived:openfda.package_ndc |
| ndc11 | package | 55910066419 | derived:openfda.package_ndc |
| ndc11 | package | 55910066469 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4c0ff1c3-8a5e-67fd-e063-6394a90ad653 | id | |
| spl set id | 1cfd85f3-ef19-46f6-8225-287a8a0a32fd | set_id | |
| unii | 3J50XA376E | openfda.unii | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | RV6J6604TK | openfda.unii | |
| unii | LAV5U5022Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reaction Since 1903 Rexall ™ is a registered trademark of Rexall Sundown, Inc. Distributed by Old East Main Co. 100 Mission Ridge Goodlettsville, TN 37072 100% Satisfaction Guaranteed! If you're not satisfied with this product for any reason, please call us so we can make you 100% satisfied. (888) 309-9030 DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.