REJUVAFLEX NATURAL PAIN RELIEVING- menthol, camphor gel
KT Marketing Group Inc.

----------

Rejuvaflex Natural Pain Relieving Gel

DRUG FACTS:

Active Ingredient:

Menthol 10.00%

Camphor 3.00%

Topical Analgesic

Indications:

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

Warnings:

For external use only.

Avoid contact with eyes.
If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

If swallowed, consult physician.
Do not apply to wounds or damaged skin.
Do not bandage tightly.

If pregnant or breast feeding,

contact physician prior ot use.

Directions:

Adults and children two-years of age or older: Apply to afftected area not more than three to four times daily.

Children under two-years of age: consult a physician.

Additional Information:

Store at room temperature.

Other Ingredients:

Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana (Arnica) Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Caprylic/Capric Triglyceride, Cetearyl Olivate, Cetyl Alcohol, Cocamidopropyl Betaine, Dimethylsulfoxide (DMSO), Ethylhexylglycerin, Glycyrrhiza Glabra (Licorice) Root Extract, Glycerin, Ilex Paraguariensis (Yerba Mate) Leaf Extract, Phenoxyethanol, Sorbitan Olivate, Xanthan Gum.

Package Labeling:

Rejuvaflex

REJUVAFLEX NATURAL PAIN RELIEVING
menthol, camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71219-782
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg in 1 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	30 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CETYL ALCOHOL (UNII: 936JST6JCN)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
GLYCERIN (UNII: PDC6A3C0OX)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SORBITAN OLIVATE (UNII: MDL271E3GR)
XANTHAN GUM (UNII: TTV12P4NEE)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71219-782-03	90 mL in 1 TUBE; Type 0: Not a Combination Product	01/02/2017	09/18/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	01/02/2017	09/18/2019

Labeler - KT Marketing Group Inc. (088915949)

Revised: 10/2023

Document Id: 074b22c1-778e-2da2-e063-6294a90aa220

Set id: 477b067c-e497-4110-e054-00144ff8d46c

Version: 3

Effective Time: 20231009

KT Marketing Group Inc.