Kaydia Pain Relieving Patches Menthol 5% Kit, 24ct

Kaydia Pain Relieving Patches Menthol 5 Kit by

Drug Labeling and Warnings

Kaydia Pain Relieving Patches Menthol 5 Kit by is a Otc medication manufactured, distributed, or labeled by Prestige Alliance Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KAYDIA PAIN RELIEVING PATCHES MENTHOL 5 KIT- menthol 
Prestige Alliance Limited

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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Kaydia Pain Relieving Patches Menthol 5% Kit, 24ct

Drug Facts

Active Ingredients:

Menthol 5%

Purpose

Pain Relieving

Use

  • For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthiritis, strains, bruises, and sprains.

Warnings

For external use only.

When using this product

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop using and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occurs again within a few days.

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 or older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: Consult a doctor.

Inactive ingredients

Activated Carbon, carbomer, Cellulose Gum, Disodium Salt, DMDM Hydantoin, Gelatin, Glycerin, Glycol Aluminum, Sodium Polyacrylate, Tartaric Acid, Water.

Package Labeling: Kit

Kit

KAYDIA PAIN RELIEVING PATCHES MENTHOL 5 KIT 
menthol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 82173-000
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82173-000-241 in 1 BOX06/01/202106/01/2021
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 112 PATCH 12 mL
Part 212 PATCH 93.6 g
Part 1 of 2
SMALL KAYDIA PAIN RELIEVING PATCHES MENTHOL 5 
menthol patch
Product Information
Item Code (Source)NDC: 82173-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
TARTARIC ACID (UNII: W4888I119H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82173-001-121 in 1 BOX
112 in 1 BAG
11 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/202106/01/2021
Part 2 of 2
LARGE KAYDIA PAIN RELIEVING PATCHES MENTHOL 5 
menthol patch
Product Information
Item Code (Source)NDC: 82173-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
TARTARIC ACID (UNII: W4888I119H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82173-002-121 in 1 BOX
112 in 1 BAG
17.8 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/202106/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/202106/01/2021
Labeler - Prestige Alliance Limited (117862948)

Revised: 7/2022