Moxie

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 (canonical bytes are SHA-256 checked before publication)

Brand name
Moxie
Generic name
ETHYL ALCOHOL
Manufacturer
Apollo Health and Beauty Care
Product type
HUMAN OTC DRUG
SPL set ID
3752d034-d4b4-47ab-b1bb-066cef7fde75
SPL ID
51177faa-2411-fc43-e063-6294a90ab0c7
Version
4
Effective date
2026-05-05
Source export date
2026-10-22
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-22/caf5811f980ee3e51e5ea59ba12f125bb3738ddeec8265aac8812df797bc62f1/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run
20261023T001338Z
Imported at
2026-10-23 00:27:16
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For External use only Flammable Keep away from source of heat or fire. When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale. Do not use on children less than 2 months of age on open skin wounds on broken or damaged skin Stop use and ask a doctor If Irritation or redness develops and lasts. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.