Herbal Utaplas External Analgesic Plaster

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
Herbal Utaplas External Analgesic Plaster
Generic name
MENTHOL, METHYL SALICYLATE
Manufacturer
Big 5 Nutrition LLC
Product type
HUMAN OTC DRUG
SPL set ID
aeaf070f-4512-4b8f-9bd8-960f6bb82881
SPL ID
0b32b98c-2483-8d0c-e063-6294a90a90b1
Version
1
Effective date
2023-11-28
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:06:32
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 Do not use ● on wounds ● irritated or damaged skin ● sensitive skin ● with a heating pad ● if pregnant ● with, or as the same time as, other external analgesic products ● if allergic to aspirin or salicylates ● if allergic to any ingredients of this product. When using this product ● avoid contact with the eyes ● do not bandage tightly ● do not apply to wounds or damaged skin ● do not use more than 3 plasters a day ● do not use 1 hour before or after bathing Stop use and ask a doctor if ● condition worsens ● symptoms persist for more than 7 days ● symptoms clear up and occur again within a few days ● excessive irritation of the skin develops ● rashes, itching or redness are present ● side effects occur. If pregnant , ask a health professional before use. Keep out of reach of children to avoid accidental poisoning. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use otherwise than as directed.

Reported adverse events (FAERS/openFDA)#

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