NDC Code(s) : 69842-053-03
Packager : CVS

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Pain Relief Lidocaine HCI LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69842-053
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE(UNII: V13007Z41A)
(LIDOCAINE - UNII:98PI200987) 		LIDOCAINE4 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF(UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL(UNII: LU49E6626Q)
CAPRYLYL TRISILOXANE(UNII: Q95M2P1KJL)
CETOSTEARYL ALCOHOL(UNII: 2DMT128M1S)
Ceteth-20 Phosphate(UNII: 921FTA1500)
DIHEXADECYL PHOSPHATE(UNII: 2V6E5WN99N)
Dimethicone(UNII: 92RU3N3Y1O)
EDETATE DISODIUM(UNII: 7FLD91C86K)
Ethylhexylglycerin(UNII: 147D247K3P)
GLYCERYL MONOSTEARATE(UNII: 230OU9XXE4)
Methylparaben(UNII: A2I8C7HI9T)
Steareth-21(UNII: 53J3F32P58)
WATER(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:69842-053-0374 mL in 1 CONTAINER Type 0: Not a Combination Product31/01/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 01/31/2017

PRINCIPAL DISPLAY PANEL

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