warnings
Warnings for this product
Original Antiseptic
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
- Original Antiseptic
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- Amazon.com Services LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 11bfc79f-ffba-45f9-82b2-a7c19b990bb2
- SPL ID
- 4c2091f5-d975-ff68-e063-6394a90a1153
- Version
- 14
- Effective date
- 2026-03-03
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:35:38
| 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 | Original Antiseptic | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Amazon.com Services LLC | openfda.manufacturer_name | |
| ndc | package | 72288-318-69 | openfda.package_ndc |
| ndc | package | 72288-318-12 | openfda.package_ndc |
| ndc | package | 72288-318-86 | openfda.package_ndc |
| ndc | package | 72288-318-77 | openfda.package_ndc |
| ndc | product | 72288-318 | openfda.product_ndc |
| ndc11 | package | 72288031886 | derived:openfda.package_ndc |
| ndc11 | package | 72288031877 | derived:openfda.package_ndc |
| ndc11 | package | 72288031869 | derived:openfda.package_ndc |
| ndc11 | package | 72288031812 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4c2091f5-d975-ff68-e063-6394a90a1153 | id | |
| spl set id | 11bfc79f-ffba-45f9-82b2-a7c19b990bb2 | 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 DISTRIBUTED BY: Amazon.com, Services, LLC Seattle, WA 98109 1-877-485-0385 ©2025 Amazon Basics Services LLC, or its affiliates. All rights reserved. www.amazon.com/amazonbasics Made in USA with U.S. and foreign components. DSP-TN-21091 DSP-MO-20087 Discard Seal, Empty & Replace Cap PLASTIC BOTTLE how2recycle.info
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.