REGENECARE HA- lidocaine hcl gel 
MPM Medical LLC

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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MP00117 MPM Regenecare HA Spray 4 fl.oz.

Active Ingredient

Lidocaine HCl 2%

Purpose

Anesthetic

Uses

For the temporary relief of pain and itching associated with

Warnings

For external use only

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

Avoid contact with the eyes

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult with a doctor

Do not use in large quantities, particularly over raw surfaces or blistered areas

Keep out of reach of children

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 physician prior to use.

Other information

Store at room temperature.

Avoid freezing and excessive heat.

Inactive ingredients

Aloe vera barbadensis leaf extract, Benzethonium chloride, Carbomer, Glycerin, Iodopropynyl butylcarbamate, Procollagen, Sodium hyaluronate, Triethanolamine, Water

Package Label

MP00117 Artwork MPM Regenecare HA Spray 4 fl.oz

REGENECARE HA 
lidocaine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66977-117
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
GLYCERIN (UNII: PDC6A3C0OX)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66977-117-04120 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/2009
Labeler - MPM Medical LLC (081241522)

Revised: 3/2022
Document Id: da2f43a6-af79-4fbc-e053-2a95a90a2029
Set id: 0eee554f-dfe0-433a-9665-8bdb95229888
Version: 2
Effective Time: 20220314
 
MPM Medical LLC