MAX-RELIEF WITH BOSWELLIA AND ALOE VERA (menthol, unspecified form and camphor- synthetic gel

Max-Relief with Boswellia and Aloe Vera by

Drug Labeling and Warnings

Max-Relief with Boswellia and Aloe Vera by is a Otc medication manufactured, distributed, or labeled by USConsultancy for Applied Research, BMC 1092, Inc. dba Solo Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts:

ACTIVE INGREDIENT

Active Ingredients:	Purpose
Camphor 6.00%	Topical Analgesic
Menthol 7.00%	Topical Analgesic

Uses

May Be Used For Relief of the Arthritis, Backache, Sprains, Strains

Other inactive ingredients

Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Boswellia Serrata Gum, Carbomer, Diazolidinyl Urea, Dimethicone, Olea Europaea (Olive) Fruit Oil, MethylParaben, Propylene Glycol, Silica, Tetrasodium EDTA, Water

Warnings

• For External Use Only! Do not use on open wounds or damaged skin. Avoid contact with eyes. Contact your physician if redness or irritation develops or if the symptoms persist or worsen.

KEEP OUT OF REACH OF CHILDREN

Directions of Use

• Apply to the affected region and massage the area till the cream disappears. Apply 3-4 times in 24 hours.

Other Information

Store in a cool place ( 15-25° C)

Questions or comments

Toll Free 1-866-222-80801
www.maxreliefglobal.com

PRINCIPAL DISPLAY PANEL - 56.7 g Tube Carton

Max-Relief
WITH BOSWELLIA & ALOE VERA

Maximum Strength, Multipurpose Ointment
For The Answer To Your Musculo-skeletal Pain

Uses For Relief of
Arthritis, Backache, Sprains and Strains

Net Weight 2OZ (56.7g)

INGREDIENTS AND APPEARANCE

MAX-RELIEF WITH BOSWELLIA AND ALOE VERA 
menthol, unspecified form and camphor (synthetic) gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71473-067
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A)	Menthol, Unspecified Form	7 g  in 100 g
Camphor (Synthetic) (UNII: 5TJD82A1ET) (Camphor (Synthetic) - UNII:5TJD82A1ET)	Camphor (Synthetic)	6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Aminomethylpropanol (UNII: LU49E6626Q)
Indian Frankincense (UNII: 4PW41QCO2M)
Carboxypolymethylene (UNII: 0A5MM307FC)
Diazolidinyl Urea (UNII: H5RIZ3MPW4)
Dimethicone (UNII: 92RU3N3Y1O)
Olive Oil (UNII: 6UYK2W1W1E)
Methylparaben (UNII: A2I8C7HI9T)
Propylene Glycol (UNII: 6DC9Q167V3)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Edetate Sodium (UNII: MP1J8420LU)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71473-067-02	1 in 1 CARTON	05/30/2017
1		56.7 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	05/30/2017

Labeler - USConsultancy for Applied Research (012848823)

Registrant - BMC 1092, Inc. dba Solo Laboratories, Inc (078831987)

Establishment
Name	Address	ID/FEI	Business Operations
BMC 1092, Inc. dba Solo Laboratories, Inc		078831987	MANUFACTURE(71473-067)