Label: ASSURED FEMININE ANTI-ITCH- benzocaine benzalkonium chloride cream
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Contains inactivated NDC Code(s)
NDC Code(s): 33992-2013-1 - Packager: Greenbrier International
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated August 8, 2016
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- Active Ingredient
- Purpose
- Uses
- Warnings
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive Ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
ASSURED FEMININE ANTI-ITCH
benzocaine benzalkonium chloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:33992-2013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 5 g in 100 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 130 mg in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) MINERAL OIL (UNII: T5L8T28FGP) HYDROXYPROPYL BISSTEARYLDIMONIUM CHLORIDE (UNII: OVB1E9X12I) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:33992-2013-1 21 g in 1 TUBE; Type 0: Not a Combination Product 02/15/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 02/15/2013 Labeler - Greenbrier International (610322518)