TJz Night-time Topical Pain Relief Balm

Manufacturer
LAB-O Corp
Effective date
2020-09-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:24

Label at a glance#

ProductTJz Night-time Topical Pain Relief Balm
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

The temporary relief of minor aches and pains of muscles and joints.

Dosage and administration

For adults and children over 12 , using the applicator tip, massage into affected area before bedtime. For children 12 years of age or younger, consult a physician before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Natural Menthol USP 2.4%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

The temporary relief of minor aches and pains of muscles and joints.

Warnings

WARNINGS SECTION

For external use only

Allergy alert: If you are allergic to aspirin or salicylates, consult a doctor before use

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • avoid contact with eyes and mucous membranes
  • wash hands with soap and water after use
  • do not apply to wounds, or damaged skin
  • do not cover with bandage or apply heat

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • redness or skin irritation occurs
  • symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

or if you have sensitive skin, ask a healthcare professional before use

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 immediately.

Flammable

SPL UNCLASSIFIED SECTION

Keep away from excessive heat or open flame

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children over 12, using the applicator tip, massage into affected area before bedtime. For children 12 years of age or younger, consult a physician before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Jojoba Seed Oil*, Beeswax*, Wintergreen Leaf Oil*, Lavender Oil*, Ginger Root Oil*, Camphor

*Organic

Other Information

OTHER SAFETY INFORMATION

Store in a cool, dry place, away from heat with lid closed tightly. Contains natural methyl salicylate from wintergreen. Report serious adverse reactions to: TJz Balm PO Box 1778, Boca Raton, FL 33429-1778 USA

Certified Organic by PCO

Company Information

SPL UNCLASSIFIED SECTION

TJzbalm.com

Questions: support@tjzbalm.com

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TJz balm

Night-time

Topical pain relief balm

Moisturizing and

Soothing

For Jaw, Neck &

Behind Ears

Hands-free,

Massaging tip applicator

A portion of the profits

will be donated to

TMJ Research

0.5 oz (14 g)

TJZ balmTJZ balm

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2397712menthol 2.4 % Topical OintmentPSN1
2397712menthol 0.024 MG/MG Topical OintmentSCD1
2397712menthol 2.4 % Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73668-001-012022-01-28C16284748780-1d6a99b39-b069-a426-e053-dadaa90af4c2TJz Night-time Topical Pain Relief Balm

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73668-001-01TJz Night-time Topical Pain Relief Balm14 g in 1 TUBE, WITH APPLICATOROINTMENT141
73668-001-01TJz Night-time Topical Pain Relief Balm1 in 1 CARTONOINTMENT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73668-001TJZ NIGHT-TIME TOPICAL PAIN RELIEF BALM (MENTHOL) OINTMENT [LAB-O CORP]1Legacy NDC, 2 package rows20200929_b055e967-d0f7-18af-e053-2995a90a1156.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73668-00173668-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b055e967-d0f8-18af-e053-2995a90a1156b055e967-d0f7-18af-e053-2995a90a11562020-09-27WarningsExact identifier
spl id: b055e967-d0f8-18af-e053-2995a90a1156
spl set id: b055e967-d0f7-18af-e053-2995a90a1156

Reported adverse events (FAERS/openFDA)#

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