Label: BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine hydrochloride cream
- NDC Code(s): 47682-260-12, 47682-260-73, 47682-260-99
- Packager: Unifirst First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 16, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
Do not use
- in the eyes
- in large quantities
- over raw surfaces or blistered areas, or on deep puncture wounds, animal bites, or serious burns
- for more than 1 week unless directed by a doctor
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- MF Burn Cream with Lidocaine Label
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INGREDIENTS AND APPEARANCE
BURN WITH LIDOCAINE
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-260 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 5 mg in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) ALCOHOL (UNII: 3K9958V90M) METHYLPARABEN (UNII: A2I8C7HI9T) ALOE VERA LEAF (UNII: ZY81Z83H0X) PARAFFIN (UNII: I9O0E3H2ZE) PETROLATUM (UNII: 4T6H12BN9U) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) WHITE WAX (UNII: 7G1J5DA97F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-260-73 25 in 1 BOX 01/24/2012 1 NDC:47682-260-99 0.9 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:47682-260-12 10 in 1 BOX 07/03/2017 2 0.9 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:47682-260-99 0.9 g in 1 PACKET; Type 0: Not a Combination Product 01/24/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/24/2012 Labeler - Unifirst First Aid Corporation (832947092)