SANA SANA Menthol External 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: SANA SANA Menthol External Analgesic
Generic name: MENTHOL
Manufacturer: Alquimia Najulam S de RL de CV
Product type: HUMAN OTC DRUG
SPL set ID: 8b7edd51-e08a-4e01-9df0-8305ce17b418
SPL ID: 3ac3eed7-e272-e15f-e063-6394a90a1d20
Version: 3
Effective date: 2025-07-25
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:31

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		SANA SANA Menthol External Analgesic	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Alquimia Najulam S de RL de CV	openfda.manufacturer_name
ndc	package	72367-000-00	openfda.package_ndc
ndc	package	72367-000-01	openfda.package_ndc
ndc	product	72367-000	openfda.product_ndc
ndc11	package	72367000000	derived:openfda.package_ndc
ndc11	package	72367000001	derived:openfda.package_ndc
rxcui		1311523	openfda.rxcui
spl id		3ac3eed7-e272-e15f-e063-6394a90a1d20	id
spl set id		8b7edd51-e08a-4e01-9df0-8305ce17b418	set_id
unii		L7T10EIP3A	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 Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days When using this product • avoid contact with eyes • do not apply to wounds or damaged skin • do not bandage tightly 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.