warnings
For external use only
AER Traveler Towelette
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
- AER Traveler Towelette
- Generic name
- AER TRAVELER
- Manufacturer
- Birchwood Laboratories LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 26556b9b-1c3a-6cf5-e063-6394a90ab26c
- SPL ID
- 47e288ba-90b4-6e1a-e063-6294a90ac823
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:56
| Harmonized routes |
|---|
| RECTAL, TOPICAL |
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 | M015 | openfda.application_number | |
| brand name | AER Traveler Towelette | openfda.brand_name | |
| generic name | AER TRAVELER | openfda.generic_name | |
| manufacturer name | Birchwood Laboratories LLC | openfda.manufacturer_name | |
| ndc | package | 50289-4200-1 | openfda.package_ndc |
| ndc | product | 50289-4200 | openfda.product_ndc |
| ndc11 | package | 50289420001 | derived:openfda.package_ndc |
| rxcui | 1247719 | openfda.rxcui | |
| rxcui | 844379 | openfda.rxcui | |
| spl id | 47e288ba-90b4-6e1a-e063-6294a90ac823 | id | |
| spl set id | 26556b9b-1c3a-6cf5-e063-6394a90ab26c | set_id | |
| unii | 101I4J0U34 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.