HealthWise Chest Rub

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
HealthWise Chest Rub
Generic name
CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL
Manufacturer
Veridian Healthcare
Product type
HUMAN OTC DRUG
SPL set ID
ce3ceffd-3ff5-3795-e053-2995a90a827f
SPL ID
48ac19dc-1140-3b99-e063-6294a90a6e19
Version
4
Effective date
2026-01-18
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:13:07
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; avoid contact with eyes. Do not use by mouth in nostrils on wounds or damaged skin with tight bandages Ask a doctor before use if you have asthma excessive phlegm (mucus) emphysema persistent or chronic cough cough associated with smoking When using this product, do not heat microwave use near open flame add to hot water or any container where heating water may cause splattering and result in burns Stop use and ask a doctor if muscle aches/pain persist more than 7 days or comes back cough lasts more than 7 days or comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center (800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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