PAIN RELIEF BALMPREFERRED PLUS PH PREFERRED PLUS PHARMACY- menthol and methyl salicylate gel 
Kinray Inc.

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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Drug Facts

Menthol 7.6%

Methyl Salicylate 29.0%

Uses

Temporarily relieves minor pain associated with:  arthritis, simple backache, muscle strains, bruises, sprains and cramps.

Warnings

For external use only.  Allergy alert:  if prone to allergic reaction from aspirin or salicylates, consult a doctor before use.  When using this product: use only as directed, avoid contact with the eyes or mucus membranes, do not bandage tightly or use with a heating pad, do not apply to wounds or damaged skin. Stop use and ask doctor if:  condition gets worse, symptoms last more than 7 days, or symptoms clear up and occur again in a few days.  If pregnant or breast-feeding:  ask a healthcare professional before use.

Directions

Adults and children 12 years of age and older:  apply generously to affected area.  Massage into painful are until thoroughly absorbed into skin.  Repeat as necessary, but not more than 4 times daily.  Children under 12 years of age: ask doctor.

Inactive ingredients

Paraffin, White Petrolatum.

Purpose

Pain relieving gel.


Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Preferred Plus Pharmacy Cool 'N Heat Therapy Pain Relief Balm

Jar image



PAIN RELIEF BALMPREFERRED PLUS PH  PREFERRED PLUS PHARMACY
menthol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:61715-020
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL .076 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE .29 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61715-020-92 99.2 g in 1 JAR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 03/15/2013
Labeler - Kinray Inc. (012574513)

Revised: 3/2013
Document Id: eeccc94f-173f-464a-848b-473ac2d480ce
Set id: a0afde4e-8fb6-4a44-85bb-b1d27a809c79
Version: 1
Effective Time: 20130315
 
Kinray Inc.