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
- Walgreen Co.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- be116a1c-697a-451b-aa2e-d39bdc2f6ff8
- SPL ID
- 4aa55136-e4d7-86c6-e063-6294a90ae9c6
- Version
- 23
- Effective date
- 2026-02-12
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:49:09
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Antispetic | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Walgreen Co. | openfda.manufacturer_name | |
| ndc | package | 0363-0664-77 | openfda.package_ndc |
| ndc | package | 0363-0664-69 | openfda.package_ndc |
| ndc | package | 0363-0664-13 | openfda.package_ndc |
| ndc | package | 0363-0664-86 | openfda.package_ndc |
| ndc | package | 0363-0664-19 | openfda.package_ndc |
| ndc | product | 0363-0664 | openfda.product_ndc |
| ndc11 | package | 00363066419 | derived:openfda.package_ndc |
| ndc11 | package | 00363066413 | derived:openfda.package_ndc |
| ndc11 | package | 00363066469 | derived:openfda.package_ndc |
| ndc11 | package | 00363066486 | derived:openfda.package_ndc |
| ndc11 | package | 00363066477 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4aa55136-e4d7-86c6-e063-6294a90ae9c6 | id | |
| spl set id | be116a1c-697a-451b-aa2e-d39bdc2f6ff8 | 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 Reactions DISTRIBUTED BY: WALGREEN CO. 200 MILMOT RD., DEERFIELD, IL 60015 walgreens.com 1-800-925-4733 DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.