MaxRevive Spray-Pain relieving spray

Manufacturer
Albert Max, Inc.
Effective date
2018-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:39:35

Label at a glance#

ProductMaxRevive Pain relieving
Active ingredientMENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE
Label structure11 sections

Indications and uses

Temporary relieves minor aches and pains of muscles and joints due to simple backache •arthritis •strains •bruises sprains

Dosage and administration

Adults and children over 2 years: Clean and dry affected area. Spray on to the area to be treated no more than 5 times a day. Children 2 years or younger: ask a doctor.

Storage and handling

Shake well before use. Close cap tightly after use Store at room temperature Keep carton. It contains important information Before using any medication, read all label information

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Methyl Salicylate 5%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relieves minor aches and pains of muscles and joints due to

  • simple backache •arthritis •strains •bruises sprains

Warnings

WARNINGS SECTION

For external use only

When Using this product

  • Use only as directed
  • do not contact with the eyes or mucous membranes
  • Do not bandage tightly.
  • Do not use on wound, irritated or broken skin.

Stop use and ask a doctor if

  • Condition worsens.
  • symptoms clear up and occur again within a few days.
  • symptoms persist for more than 7 days.
  • skin rash occurs or excessive irritation of the skin develops.

If pregnant or breast feeding, ask a doctor 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years: Clean and dry affected area. Spray on to the area to be treated no more than 5 times a day.

Children 2 years or younger: ask a doctor.

Other Information

STORAGE AND HANDLING SECTION

  • Shake well before use. Close cap tightly after use
  • Store at room temperature
  • Keep carton. It contains important information
  • Before using any medication, read all label information

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Saposhnikoviae Radix, Artemisia Argyi Leaf, Moutan Cortex, Carpesii Fructus, Cimicifugae Rhizoma, Sophorae Flavescentis Radix, Impatiens Balsamina, Paeoniae Rubra Radix, Zanthoxyli Pericarpium, Glycyrrhizae Radix Et Rhizoma, Notoginseng Radix Et Rhizoma, Carthami Flos, Ethyl Alcohol.

Questions or Comments?

OTC - QUESTIONS SECTION

Call:1-800-617-2021

SPL UNCLASSIFIED SECTION

Distributed by

Albert Max, Inc

Chino, CA 91710

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68233-805-012023-10-10C16284748780-1d6a99b39-9dec-a426-e053-dadaa90af4c2MaxRevive Spray-Pain relieving spray
68233-805-012022-01-28C16284748780-1d6a99b39-9dec-a426-e053-dadaa90af4c2MaxRevive Spray-Pain relieving spray

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68233-80568233-805-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
0756f58d-aac9-778c-e063-6294a90ae4f25bd3acd8-334d-4775-ab6a-7ac9f9dbc0c12023-10-10WarningsExact identifier
spl set id: 5bd3acd8-334d-4775-ab6a-7ac9f9dbc0c1

Reported adverse events (FAERS/openFDA)#

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