MERCY PAIN RELIEVING- menthol lotion

MERCY PAIN RELIEVING by

Drug Labeling and Warnings

MERCY PAIN RELIEVING by is a Otc medication manufactured, distributed, or labeled by Cloud 9 Naturally. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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.

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

MERCY PAIN RELIEVING 
menthol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72070-100
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	1.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
OLIVE OIL (UNII: 6UYK2W1W1E)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72070-100-01	113.4 g in 1 BOTTLE; Type 0: Not a Combination Product	05/18/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/18/2018

Labeler - Cloud 9 Naturally (255353633)

Establishment
Name	Address	ID/FEI	Business Operations
Cloud 9 Naturally		255353633	manufacture(72070-100)