MERCY PAIN RELIEVING- menthol lotion 
Cloud 9 Naturally

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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MERCY PAIN RELIEVING LOTION

Drug Facts

Active ingredient

Menthol 1.3%

Purpose

Topical Analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints associated with

• simple backache • arthritis  • strains • bruises • sprains

Warnings

For external use only

When using this product

• avoid contact with the eyes and mucous membranes

• do not apply to wounds or damaged skin

• do not bandage tightly

Stop use and ask a doctor if

• condition worsens

• symptoms persist for more than 7 days

• clear up and occur again within a few days

If pregnant or breast-feeding, consult a health professional 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 2 years of age and older: apply to affected area not more than 3 to 4 times daily.

• children under 2 years of age: consult a doctor.

Inactive ingredients

Cetyl Alcohol, Fragrance, Glycerin, Methylsulfonylmethane (MSM), Olive (Oleo Europaea) Oil, Stearic Acid, Water

Other information

do not use if seal or cap is broken.

Questions?

1-403-348-9704, Mon-Fri, 9AM to 5 PM.

You may also report serious side effects to this phone number.

Soothes minor pain of

• muscles • joints • backache • arthritis 

Manufactured by:

Cloud 9 Naturally Inc,

53840 National Rd, Lower unit,

Bridgeport, Ohio, 43912 USA

www.cloud9naturally.com

Packaging

Mercy Pain Relieving Lotion

MERCY PAIN RELIEVING 
menthol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72070-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM1.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72070-100-01113.4 g in 1 BOTTLE; Type 0: Not a Combination Product05/18/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/18/2018
Labeler - Cloud 9 Naturally (255353633)
Establishment
NameAddressID/FEIBusiness Operations
Cloud 9 Naturally255353633manufacture(72070-100)

Revised: 5/2018
Document Id: 8c6e9a62-838e-4231-8ead-3ea8b76febd5
Set id: aa584c8f-ab36-474d-af63-49471b900a21
Version: 2
Effective Time: 20180518
 
Cloud 9 Naturally