Tei-Fu recovery Massage Lotion

Manufacturer
Wasatch Product Development
Effective date
2025-10-10
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:38:33

Label at a glance#

ProductTe-Fu Recovery Massage
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Menthol (5.0%) Topical Analgesic

Methyl Salicylicate (10%) Topical Analgesic

OTC - PURPOSE SECTION

Uses

Provides warming, penetrating pain relief for sore muscles and joints

May also provide temporary relief of minor aches and pains associated with backache, strains and bruises

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of product and consult a physician.

WARNINGS SECTION

Warnings

For external use only.

Avoid contact with eyes

Do not bandage tightly

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 2 year of age and older apply to affected area not more than 3 to 4 times per day

Children under 2yrs of age consult a physician.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Cinnamomium Camphora (Camphor) Bark Oil, Stearyl Alcohol, C13-15 Alkane, Glycerin, Caprylic/capric Triglyceride, Pentylene Glycol, Glyceryl Stearate, Cetearyl Alcohol, Eucalyptus Globulus Leaf Oil, Prunus Amygdalus Dulcis( sweet almond) Oil, Microcrystalline Cellulose, Mentha Piperita (peppermint) Oil, Behenyl Alcohol, Stearyl Phosphate, Eugenia Caryophyllus (Clove) Leaf Oil, Hydroxyacetophenone, Zingiber Officinale (ginger) Root Oil, Arnica Montana Flower Extract, Benzyl Alcohol, Cellulose Gum, Cyamopsis Tetragonoloba (Guar) Gum, Xanthan Gum, Sodium Phytate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tei-Fu

Recovery Massage Lotion

Penetrating Muscle and Joint Relief

4fl. oz. ( 118 mL)

boxbox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2105550menthol 5 % / methyl salicylate 10 % Topical LotionPSN5
2105550menthol 50 MG/ML / methyl salicylate 100 MG/ML Topical LotionSCD5
2105550menthol 5 % / methyl salicylate 10 % Topical LotionSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130099904219137GTIN-13: 0099904219137
EAN-13: 0099904219137
GTIN-12: 099904219137
UPC-A: 099904219137
GTIN storage (14 digits): 00099904219137
4 OZ TEI-FU RECOVERY MESSAGE LOTION LUS21913 REV 0718 copy.jpg
Data codeITF0102191307184 OZ TEI-FU RECOVERY MESSAGE LOTION LUS21913 REV 0718 copy.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44717-539-01Te-Fu Recovery Massage118 mL in 1 BOTTLELOTION1185

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44717-53944717-539-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-22full-release2026-06-01 00:28:33

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
Te-Fu Recovery MassageMENTHOL, METHYL SALICYLATEWasatch Product Development7bc2989f-dfb6-e8af-e053-2991aa0a0bf22025-10-10WarningsExact identifier
ndc (package): 44717-539-01
ndc (product): 44717-539
ndc11 (package): 44717053901
spl id: 40d36d7b-8ff4-0714-e063-6394a90a1fcd
spl set id: 7bc2989f-dfb6-e8af-e053-2991aa0a0bf2

Reported adverse events (FAERS/openFDA)#

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