Family Care Pain Relief

Manufacturer
United Exchange Corporation
Effective date
2018-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:57:06

Label at a glance#

ProductFamily Care Pain Relief
Active ingredientMENTHOL
Label structure14 sections

Storage and handling

store at room temperature 20-25°C (68-77°F) protect from excessive heat

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Menthol 2%.........................Topical analgesic

OTC - PURPOSE SECTION

Uses

  • Temporarily relieves the minor aches and pains of muscles and joints associated with:
  • sprains
  • simple backache
  • arthritis
  • strains
  • bruises

WARNINGS SECTION

Warnings

For external use only

Allergy alert: If prone to allergic reaction from aspirin or slicylates, consult a doctor before use.

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product
  • on a child under 12 years of age with arthritis-like conditions

DOSAGE & ADMINISTRATION SECTION

Distributed By:

UNITED EXCHANGE CORPORATION

Cypress, CA. 90630 USA | 1-888-645-8204 | Made in China

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have redness over the affected area.

OTC - WHEN USING SECTION

When using this product

  • use only as directed
  • avoid contact with eyes, mucous membranes or rashes
  • do not bandage tightly
  • discontinue use at least 1 hour before a bath or shower
  • do not use immediately after a bath or shower

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • redness is present or irritation or rash develops
  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE SECTION

Directions

  • adults and children 12 years of age and older:
  • clean and dry affected area
  • apply generously to affected area
  • massage into painful area until thoroughly absorbed into skin
  • repeat as necessary, but not more than 4 times daily
  • children under 12 years of age: consult a doctor

STORAGE AND HANDLING SECTION

  • store at room temperature 20-25°C (68-77°F)
  • protect from excessive heat

INACTIVE INGREDIENT SECTION

Inactive ingredients alcohol, hydrogenated castor oil, methyl salicylate, peg-150 distearate, propylene glycol, purified water, sodium stearate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9012090120

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2099927menthol 2 % Topical OintmentPSN1
2099927menthol 0.2 MG/MG Topical OintmentSCD1
2099927menthol 0.2 MG/MG Topical StickSY1
2099927menthol 2 % Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65923-119-012022-01-28C16284748780-1d6a99b39-6949-a426-e053-dadaa90af4c2Coralite Pain Relief Stick 1.75oz (90120, 2018)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65923-119-01Family Care Pain Relief0.02 g in 1 TUBESTICK0.021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65923-119FAMILY CARE PAIN RELIEF (MENTHOL) STICK [UNITED EXCHANGE CORPORATION]1Legacy NDC, 1 package rows20181031_79778b06-78d5-c616-e053-2a91aa0a78f8.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65923-11965923-119-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
79778b06-78d6-c616-e053-2a91aa0a78f879778b06-78d5-c616-e053-2a91aa0a78f82018-10-30WarningsExact identifier
spl id: 79778b06-78d6-c616-e053-2a91aa0a78f8
spl set id: 79778b06-78d5-c616-e053-2a91aa0a78f8

Reported adverse events (FAERS/openFDA)#

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