NDC Code(s) : 69998-160-01, 69998-160-02
Packager : Benton Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

ALOE PROPOLIS SOOTHING GE LAllantoin GEL
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69998-160
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Allantoin(UNII: 344S277G0Z)
(ALLANTOIN - UNII:344S277G0Z) 		Allantoin0.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF(UNII: ZY81Z83H0X)
PROPOLIS WAX(UNII: 6Y8XYV2NOF)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:69998-160-021 in 1 CARTON 12/01/2016
1NDC:69998-160-01100 mL in 1 TUBE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 12/01/2016

PRINCIPAL DISPLAY PANEL

Image of carton