FDA.reportPublic FDA data

SANA SANA Menthol External Analgesic

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical 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
2026-08-01
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/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:27:48
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 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.