Valtrum 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 TOPICAL ANALGESIC
Generic name: CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer: Laboratorios Quantium LLC
Product type: HUMAN OTC DRUG
SPL set ID: f3c4cc3a-f3a3-4d02-97e0-9c3fc1a67c3e
SPL ID: ac0795eb-ebb6-4828-98fa-371e1a716c99
Version: 1
Effective date: 2026-05-13
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:03:41

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 TOPICAL ANALGESIC	openfda.brand_name
generic name		CAMPHOR, MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		Laboratorios Quantium LLC	openfda.manufacturer_name
ndc	package	75849-031-31	openfda.package_ndc
ndc	product	75849-031	openfda.product_ndc
ndc11	package	75849003131	derived:openfda.package_ndc
rxcui		2673206	openfda.rxcui
spl id		ac0795eb-ebb6-4828-98fa-371e1a716c99	id
spl set id		f3c4cc3a-f3a3-4d02-97e0-9c3fc1a67c3e	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.