NEILMED HOT AND COLD PAIN RELIEF- pain relief spray spray 
NeilMed Pharmaceuticals Inc.

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NeilMed Hot and Cold Pain Relief Spray

Directions

Directions: Shake well – adults and children 12 years of age and older: spray product on affected area, not more than 3 to 4 times daily. – children under 12 years of age: consult a doctor.

Warnings


For external use only.
Flammable: Do not use while smoking or near heat or flames. Avoid long term storage above 104°F. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.
When using this product avoid contact with eyes and mucous membranes. Do not apply to wounds or damaged skin. Do not bandage tightly. Use only as directed.
Stop use and ask doctor if condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. Do not use for longer than 1 week.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
If pregnant or breast-feeding, ask a health professional before use.

Inactive Ingredients

Glycerin, Propylene Glycol, SD Alcohol 40 (58%), USP grade Purified Water.

Uses

Temporarily alleviates minor aches and pains of muscles and joints associated with Arthritis, Simple Backache, Strains, Bruises, or Sprains

Warnings:
Keep out of reach of children.

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

Drug Facts:

Topical Analgesic

Drug Facts:

Active Ingredient

Menthol 16.0%

Package Label - NeilMed Hot & Cold Pain Relief

NeilMed Hot & Cold Pain Relief Spray

NEILMED HOT AND COLD PAIN RELIEF 
pain relief spray spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13709-238
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.16 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:13709-238-01118 g in 1 CAN; Type 0: Not a Combination Product11/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/11/2020
Labeler - NeilMed Pharmaceuticals Inc. (799295915)
Establishment
NameAddressID/FEIBusiness Operations
NeilMed Pharmaceuticals, Inc799295915manufacture(13709-238)

Revised: 1/2024
Document Id: 0eb0c83d-d076-1c8f-e063-6294a90a1423
Set id: b3d02111-7499-c2d4-e053-2a95a90ae1de
Version: 3
Effective Time: 20240111
 
NeilMed Pharmaceuticals Inc.