Label: LANACANE MAXIMUM STRENGTH ANTI-ITCH- benzethonium chloride and benzocaine cream
- NDC Code(s): 63824-810-01
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 29, 2023
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Inactive ingredients
acetylated lanolin alcohol, aloe, cetyl acetate, cetyl alcohol, cholecalciferol, corn oil, dimethicone, dl-alpha tocopherol acetate, fragrance, glycerin, glyceryl monostearate, isopropyl myristate, methylparaben, mineral oil, PEG-100 stearate, polyvinylpyrrolidone/eicosene copolymer, propylparaben, pyrithione zinc, retinyl palmitate, sorbitan monostearate, stearamidopropyl PG-dimonium chloride phosphate, water
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PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
NDC 63824-810-01
LANACANE ®
Maximum Strength
ANTI-ITCH
CREAMBenzethonium chloride 0.2%
(First-Aid Antiseptic)
Benzocaine 20%
(Pain Relieving Cream)2-in-1
FAST Acting
Itch Relief+
Kills Germs*
*unlike HydrocortisonesTemporary itch relief from:
- Insect bites
- Rashes
- Dry, Itchy skin
NET WT. 1 OZ (28 g)
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INGREDIENTS AND APPEARANCE
LANACANE MAXIMUM STRENGTH ANTI-ITCH
benzethonium chloride and benzocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-810 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 2 mg in 1 g BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg in 1 g Inactive Ingredients Ingredient Name Strength ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) ALOE (UNII: V5VD430YW9) CETYL ACETATE (UNII: 4Q43814HXS) CETYL ALCOHOL (UNII: 936JST6JCN) CHOLECALCIFEROL (UNII: 1C6V77QF41) CORN OIL (UNII: 8470G57WFM) DIMETHICONE (UNII: 92RU3N3Y1O) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PEG-100 STEARATE (UNII: YD01N1999R) PROPYLPARABEN (UNII: Z8IX2SC1OH) PYRITHIONE ZINC (UNII: R953O2RHZ5) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) STEARAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-810-01 1 in 1 CARTON 09/28/2012 08/25/2025 1 28 g 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 Drug M003 09/28/2012 08/25/2025 Labeler - RB Health (US) LLC (081049410)