SANA SANA Menthol External Analgesic

Manufacturer
Alquimia Najulam S de RL de CV
Effective date
2025-07-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:08:39

Label at a glance#

ProductSANA SANA Menthol External Analgesic
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with • simple backache • arthritis • strains • bruises • sprains

Dosage and administration

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 15%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with
• simple backache
• arthritis
• strains
• bruises
• sprains

Warnings

WARNINGS SECTION

For external use only

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens

• symptoms persist for more than 7 days or clear up and occur again within a few days

When using this product

OTC - WHEN USING SECTION

• avoid contact with eyes

• do not apply to wounds or damaged skin

• do not bandage tightly

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

• children under 2 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

ionized water, glycerin, triethanolamine, carbopol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label02Label02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1311523menthol 15 % Topical GelPSN3
1311523menthol 0.15 MG/MG Topical GelSCD3
1311523menthol 15 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72367-000-002025-07-25C16284748780-19d75b9cf-fa9d-f424-e053-dadaa90a57ceSANA SANA Menthol External Analgesic
72367-000-002020-01-31C16284748780-19d75b9cf-fa9d-f424-e053-dadaa90a57ceSANA SANA Menthol External Analgesic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72367-000-00SANA SANA Menthol External Analgesic240 g in 1 BOTTLEGEL2403
72367-000-00SANA SANA Menthol External Analgesic1 in 1 BOXGEL13
72367-000-01SANA SANA Menthol External Analgesic240 g in 1 BOTTLE, PUMPGEL2403

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72367-00072367-000-00, 72367-000-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SANA SANA Menthol External AnalgesicMENTHOLAlquimia Najulam S de RL de CV8b7edd51-e08a-4e01-9df0-8305ce17b4182025-07-25WarningsExact identifier
ndc (package): 72367-000-00
ndc (package): 72367-000-01
ndc (product): 72367-000
ndc11 (package): 72367000000
ndc11 (package): 72367000001
spl id: 3ac3eed7-e272-e15f-e063-6394a90a1d20
spl set id: 8b7edd51-e08a-4e01-9df0-8305ce17b418

Reported adverse events (FAERS/openFDA)#

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