Label: RED CROSS CANKER SORE- benzocaine ointment
- NDC Code(s): 10742-8915-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Active ingredient
- Purpose
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Warnings
Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops: ▪ pale, gray, or blue colored skin (cyanosis) ▪ headache ▪ rapid heart rate ▪ shortness of breath ▪ dizziness or lightheadedness ▪ fatigue or lack of energy
Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other “caine” anesthetics
- Keep Out of Reach of Children
- Directions
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Inactive Ingredients
aloe barbadensis leaf extract, butylated hydroxytoluene, carbomer hompolymer, cetylpyridinium chloride, chamomilla recutita (matricaria) flower extract, cocos nucifera (coconut) oil, commiphora myrrha resin, dimethicone, echinacea purpurea extract, flavor, glyceryl stearate, menthol, mineral oil, silica dimethicone silylate, vitamin E, white petrolatum
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INGREDIENTS AND APPEARANCE
RED CROSS CANKER SORE
benzocaine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-8915 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) CHAMOMILE (UNII: FGL3685T2X) COCONUT OIL (UNII: Q9L0O73W7L) MYRRH (UNII: JC71GJ1F3L) ECHINACEA PURPUREA (UNII: QI7G114Y98) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) MINERAL OIL (UNII: T5L8T28FGP) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-8915-1 1 in 1 BLISTER PACK 08/19/1998 1 7 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 M022 08/19/1998 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-8915)