MAXREVIVE PAIN RELIEVING- menthol, methyl salicylate spray

MaxRevive by

Drug Labeling and Warnings

MaxRevive by is a Otc medication manufactured, distributed, or labeled by Albert Max, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

SPL UNCLASSIFIED SECTION

Distributed by

Albert Max, Inc

Chino, CA 91710

Packaging

INGREDIENTS AND APPEARANCE

MAXREVIVE   PAIN RELIEVING
menthol, methyl salicylate spray

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

Inactive Ingredients
Ingredient Name	Strength
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)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2003

Labeler - Albert Max, Inc. (149445798)