MaxRevive Spray-Pain relieving spray

Drug Facts

Active Ingredients

Menthol 10%

Methyl Salicylate 5%

Purpose

External analgesic

Uses

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

simple backache •arthritis •strains •bruises sprains

Warnings

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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

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

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?

Call:1-800-617-2021

Distributed by

Albert Max, Inc

Chino, CA 91710

Packaging

image description

MAXREVIVE PAIN RELIEVING
menthol, methyl salicylate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:68233-805
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	0.1 g in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	0.05 g in 1 mL

Ingredient Name	Strength
Inactive Ingredients
SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)
PAEONIA X SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X)
CARPESIUM ABROTANOIDES FRUIT (UNII: 20C78R73NH)
ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
IMPATIENS BALSAMINA WHOLE (UNII: ZMK32KX641)
PAEONIA OBOVATA ROOT (UNII: 7NPF74465O)
ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
LICORICE (UNII: 61ZBX54883)
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
SAFFLOWER (UNII: 4VBL71TY4Y)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:68233-805-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2003	10/10/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	09/01/2003	10/10/2023

Labeler - Albert Max, Inc. (149445798)

Revised: 10/2023

Document Id: 0756f58d-aac9-778c-e063-6294a90ae4f2

Set id: 5bd3acd8-334d-4775-ab6a-7ac9f9dbc0c1

Version: 4

Effective Time: 20231010

Albert Max, Inc.