NDC Code(s) : 68093-7079-3
Packager : Wisconsin Pharmacal Company

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

VH Essentials Benzocaine, Benzalkonium Chloride CREAM
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68093-7079
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzocaine(UNII: U3RSY48JW5)
(Benzocaine - UNII:U3RSY48JW5) 		Benzocaine.05 g in 1 g
Benzalkonium Chloride(UNII: F5UM2KM3W7)
(Benzalkonium - UNII:7N6JUD5X6Y) 		Benzalkonium Chloride.0013 g in 1 g
Inactive Ingredients
Ingredient Name Strength
Aloe Vera Leaf(UNII: ZY81Z83H0X)
Carbomer Homopolymer Type C (Allyl Pentaerythritol Crosslinked)(UNII: 4Q93RCW27E)
Cetyl Alcohol(UNII: 936JST6JCN)
Water(UNII: 059QF0KO0R)
Glyceryl Monostearate(UNII: 230OU9XXE4)
Isopropyl Palmitate(UNII: 8CRQ2TH63M)
Isopropyl Stearate(UNII: 43253ZW1MZ)
Lanolin Alcohols(UNII: 884C3FA9HE)
Methylparaben(UNII: A2I8C7HI9T)
Mineral Oil(UNII: T5L8T28FGP)
PEG-100 Stearate(UNII: YD01N1999R)
Propylparaben(UNII: Z8IX2SC1OH)
.Alpha.-Tocopherol Acetate(UNII: 9E8X80D2L0)
Trolamine(UNII: 9O3K93S3TK)
Trisodium HEDTA(UNII: K3E0U7O8KI)
Isopropyl Myristate(UNII: 0RE8K4LNJS)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:68093-7079-31 in 1 CARTON
142.5 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 12/01/2010

PRINCIPAL DISPLAY PANEL

ArtworkImage of tube

PRINCIPAL DISPLAY PANEL

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