NDC Code(s) : 63742-004-00, 63742-004-01
Packager : Clinical Resolution Laboratory, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Numb SootheLidocaine CREAM
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63742-004
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE(UNII: 98PI200987)
(LIDOCAINE - UNII:98PI200987) 		LIDOCAINE50 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
ALOE VERA LEAF(UNII: ZY81Z83H0X)
CHAMOMILE(UNII: FGL3685T2X)
TROLAMINE(UNII: 9O3K93S3TK)
CARBOXYPOLYMETHYLENE(UNII: 0A5MM307FC)
DIETHYLENE GLYCOL MONOETHYL ETHER(UNII: A1A1I8X02B)
NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE(UNII: VLW429K27K)
TRIDECETH-10(UNII: G624N6MSBA)
.ALPHA.-TOCOPHEROL ACETATE(UNII: 9E8X80D2L0)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:63742-004-008 g in 1 BOTTLE Type 0: Not a Combination Product01/01/2018
2NDC:63742-004-0115 g in 1 BOTTLE Type 0: Not a Combination Product01/01/2018
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part346 01/01/2018

PRINCIPAL DISPLAY PANEL

63742-004-00

PRINCIPAL DISPLAY PANEL

63742-004-01