Label: FIRST AID BURN- lidocaine hydrochloride,benzalkonium chloride cream
- NDC Code(s): 82749-009-01
- Packager: Epic Medical Supply Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 4, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use- in the eyes
- over large areas of the body or on deep puncture wounds, animal bites, or serious burns
- in large quantities, particularly over raw surfaces or blistered areas
Stop use and ask a doctor if
- the condition gets worse
- condition clears up and recurs within a few days
- condition persists for more than 7 days
- If pregnant or breast feeding, ask a health care professional before use.
- Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Questions?
- Product label
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INGREDIENTS AND APPEARANCE
FIRST AID BURN
lidocaine hydrochloride,benzalkonium chloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82749-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 5 mg in 1 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H) WATER (UNII: 059QF0KO0R) METHYLPARABEN SODIUM (UNII: CR6K9C2NHK) PROPYLPARABEN SODIUM (UNII: 625NNB0G9N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82749-009-01 144 in 1 BOX 06/01/2024 1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 06/01/2024 Labeler - Epic Medical Supply Corp (101423894)