Label: REGENECARE HA- lidocaine hcl gel
- NDC Code(s): 66977-107-03
- Packager: MPM Medical LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 17, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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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
- Directions
- Other information
- Inactive ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
REGENECARE HA
lidocaine hcl gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66977-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W) ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZETHONIUM CHLORIDE (UNII: PH41D05744) CARBOMER 940 (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) HYALURONATE SODIUM (UNII: YSE9PPT4TH) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66977-107-03 85 g in 1 TUBE; Type 0: Not a Combination Product 01/05/2007 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 01/05/2007 Labeler - MPM Medical LLC (081241522)