FDA.reportPublic FDA data

Camphotrex

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
Camphotrex
Generic name
CAMPHOR, MENTHOL
Manufacturer
PureTek Corporation
Product type
HUMAN OTC DRUG
SPL set ID
3b6c6eef-e92d-497d-afe8-82356637c2b8
SPL ID
1e2d1f71-9f7b-e353-e063-6294a90a4a2c
Version
5
Effective date
2024-07-26
Source export date
2026-08-01
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/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:03:51
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 Do not use on ■ wounds ■ damaged skin When using this product ■ avoid getting into eyes or mucous membranes ■ do not bandage tightly Stop use and ask a doctor if ■ excessive irritation of the skin develops ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.