FDA.reportPublic FDA data

MAX REVIVE

Manufacturer
Big 5 Nutrition LLC
Effective date
2026-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-10-24 01:01:01

Label at a glance#

ProductMax Revive Plaster
Active ingredientMENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE
Label structure10 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: ■ arthritis ■ strains ■ bruises ■ sprains ■ simple backache

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Menthol 5%

Methyl Salicylate 1%

OTC - PURPOSE SECTION

Purpose

External Analgesic

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

■ arthritis

■ strains

■ bruises

■ sprains

■ simple backache

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ on wounds

■ irritated or damaged skin

■ sensitive skin

■ with a heating pad

■ if pregnant

■ with, or as the same time as, other external analgesic products

■ if allergic to aspirin or salicylates

■ if allergic to any ingredients of this product

When using this product

OTC - WHEN USING SECTION

■ avoid contact with the eyes
■ do not bandage tightly
■ do not apply to wounds or damaged skin
■ do not use more than 3 plasters a day
■ do not use 1 hour before or after bathing

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens
■ symptoms persist for more than 7 days
■ symptoms clear up and occur again within a few days
■ excessive irritation of the skin develops
■ rashes, itching or redness are present
■ side effects occur

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning.

In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use otherwise than as directed.

DOSAGE & ADMINISTRATION SECTION

Directions

■ Adults and children 12 years of age and older: clean and dry affected area. Remove plaster from the protective layer, apply to the affected area, rub the area     with your hand to secure the patch.
■ Plaster will remain effective for 8 hours.
■ Avoid using the same patch on the same area for more than 2 days.
■ Do not apply to area with excessive hair. Adhesive plaster may hurt skin upon removal.
■ Wet patch with warm water before removing from skin.
■ Children under 12 years of age: Do not use or consult a doctor.

Other Information

OTHER SAFETY INFORMATION

■ Store unused patch in the pouch
■ Store at room temperature, 20 to 25°C (68 to 77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Chinese Clematidis Root & Rhizome,Yellow wax, Momordica cochinchinensis seeds, Castor Seeds, Myrrh, Frankincense, Sesame Oil, Resin, FD&C Blue No. 2, FD&C Yellow No. 5, Zinc Oxide

Questions or Comments

OTC - QUESTIONS SECTION

Call: 1-800-617-2021

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82198-001982198-0019-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
CLEMATIS CHINENSIS ROOT8Z18N528CUIACT
YELLOW WAX2ZA36H0S2VIACT
MOMORDICA COCHINCHINENSIS SEED2T87O1UPVDIACT
RICINUS COMMUNIS SEED7EK4SFN1TXIACT
MYRRHJC71GJ1F3LIACT
FRANKINCENSER9XLF1R1WMIACT
SESAME OILQX10HYY4QVIACT
PINUS MASSONIANA RESIN64S07U83T7IACT
FD&C BLUE NO. 2L06K8R7DQKIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
ZINC OXIDESOI2LOH54ZIACT

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 4 · 64 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Meriwether Skin Pain ReliefMENTHOL, UNSPECIFIED FORMMeriwether Skin LLCf6e155be-5879-4176-bb0e-e364f2e5cdf92026-07-16WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Propolis Cooling Relief Cherry Cough DropsMENTHOL, UNSPECIFIED FORMBeekeeper's Naturals USA Inc7087566d-f24a-4508-aa25-7f42d055c43e2026-07-13WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC00bba5d2-b0e0-701c-e063-6294a90a57412026-05-15WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze Overnight ReliefMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC07be6e88-1850-4d6a-946d-f03830b8c4a22026-05-15WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC6bef9ccb-7a5a-4c67-b1bc-a92b167312da2026-05-15WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze ProfessionalMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCdb982baf-31ea-4f09-90e3-cd5facb5dfe52026-05-15WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze Professional Roll-OnMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCf62f8ec3-593d-480a-85a0-01fcd7f1790c2026-05-15WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze MentholMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLC3f2b1f48-2d78-4985-a046-9f72de5e1a9b2026-05-13WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze Professional ColorlessMENTHOL, UNSPECIFIED FORMReckitt Benckiser4639201c-a67a-475f-8df6-3dc6225803ad2026-05-12WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Biofreeze Professional Colorless Roll-OnMENTHOL, UNSPECIFIED FORMReckitt Benckiser LLCbae9946a-4c68-4759-9fb3-0a61a7ad0eb72026-05-12WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
24 7 Relief and Recovery Pain RelievingMENTHOL, UNSPECIFIED FORMTriplicare Inc53ca807b-3ec2-4b5e-aa5a-6dcb756bb4232026-04-30WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Stopain ClinicalMENTHOL, UNSPECIFIED FORMTroy Manufacturing, Inc.4503208f-2808-4727-8066-c431230bd70b2026-04-16WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
BonicaEaseX 24 Hour Menthol Pain RelievingMENTHOL, UNSPECIFIED FORMPlanet (Anhui) Pharmaceutical Co., Ltd.17fc0cd1-710d-45e6-9513-d7100e3adb422026-04-10WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
BonicaEaseX Colorless Roll-On Menthol Pain RelievingMENTHOL, UNSPECIFIED FORMPlanet (Anhui) Pharmaceutical Co.,Ltdacf460b4-1b41-4b30-a74a-6c3613119d8e2026-04-10WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
BonicaEaseX Menthol Pain RelievingMENTHOL, UNSPECIFIED FORMPlanet (Anhui) Pharmaceutical Co.,Ltd4d84b4fb-8f55-4b2b-b261-858edb7f31442026-04-10WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Topical Hemorrhoid Relief GelMENTHOL, UNSPECIFIED FORMYantai Aien Biotechnology Co., Ltd.4d6e6667-ab1c-de7c-e063-6294a90a0b9b2026-03-20WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
CVS Health Pain Relief FootMENTHOL, UNSPECIFIED FORMNATURAL ESSENTIALS, INC.0f646876-69d0-49db-ade2-2b3eb26dd3992026-03-16WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
Still StandingMENTHOL, UNSPECIFIED FORMNatural Essentials Inc.66974aaf-c82f-4fe9-bfb3-3430b80ac9f22026-03-02WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
daily solutions Ice Blue AnalgesicMENTHOL, UNSPECIFIED FORMGarcoa, Inc.4d8c8c14-ecaa-43de-a07f-c73ca0d1e3e62026-02-06WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM
FEMININE PAIN RELIEFMENTHOL, UNSPECIFIED FORMBeYou Together Ltd9636b973-fe7e-481e-a6e9-8070347c08832025-12-31WarningsName fallback
generic name: MENTHOL, UNSPECIFIED FORM

Reported adverse events (FAERS/openFDA)#

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