Menthol Camphor Cough Suppressant Topical Analgesic 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
Menthol Camphor Cough Suppressant Topical Analgesic Rub
Generic name
CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM
Manufacturer
J.R. Watkins, LLC.
Product type
HUMAN OTC DRUG
SPL set ID
fd0ea70a-ef12-48b1-8d9d-cc5f6417f854
SPL ID
10e11e75-6321-b9b4-e063-6394a90a0e63
Version
2
Effective date
2024-02-08
Source export date
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:45
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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 a tight bandage Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) chronic cough that lasts such as occurs with smoking, asthma, or emphysema When using this product, do not heat microwave 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 and pains last more than 7 days or clear up and occur again within a few days cough last more than 7 days, comes back or occurs with fever, rash, or persistent headache. These could be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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