Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC

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: Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC
Generic name: CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer: LABORATORIOS QUANTIUM LLC
Product type: HUMAN OTC DRUG
SPL set ID: c4efa317-8dd1-49e1-b7ca-9df2147edd3e
SPL ID: d492a160-8eea-49bf-a0fa-b918c9aec441
Version: 1
Effective date: 2023-12-21
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:52:01

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC	openfda.brand_name
generic name		CAMPHOR, MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		LABORATORIOS QUANTIUM LLC	openfda.manufacturer_name
ndc	package	75849-897-03	openfda.package_ndc
ndc	product	75849-897	openfda.product_ndc
ndc11	package	75849089703	derived:openfda.package_ndc
rxcui		2673206	openfda.rxcui
spl id		d492a160-8eea-49bf-a0fa-b918c9aec441	id
spl set id		c4efa317-8dd1-49e1-b7ca-9df2147edd3e	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		LAV5U5022Y	openfda.unii

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 and mucous membranes • Do not use otherwise than as directed. Caution: Discontinue use if excessive irritation of the skin develops. When using this product: • Do not bandage tightly • Do not apply to wounds or damaged skin. Stop use and ask a doctor if: • Conditions worsens • Symptoms persist for 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.

Reported adverse events (FAERS/openFDA)#

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