HIMARK

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
HIMARK
Generic name
ALCOHOL
Manufacturer
Apollo Health and Beauty Care
Product type
HUMAN OTC DRUG
SPL set ID
f9658a02-e3fa-096a-e053-6294a90afb21
SPL ID
50efa4a3-b312-b55f-e063-6394a90a2dc3
Version
4
Effective date
2026-05-03
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:28:41
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. Do not use On infants less than 2 months of age. On open skin wounds On broken or damaged skin. When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale. 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 Center immediately.

Reported adverse events (FAERS/openFDA)#

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