Label: FIRST AID AND BURN- benzalkonium chloride, lidocaine hydrochloride cream
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Contains inactivated NDC Code(s)
NDC Code(s): 0924-5701-01, 0924-5701-05, 0924-5701-06, 0924-5701-07, view more0924-5701-08 - Packager: Acme United Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 24, 2012
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- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Keep out of reach of children.
If ingested, get medical help or contact a Poison Control Center right away.
- Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL – Pac-Kit 12 count box
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INGREDIENTS AND APPEARANCE
FIRST AID AND BURN
benzalkonium chloride, lidocaine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0924-5701 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 5 mg in 1 g Inactive Ingredients Ingredient Name Strength aloe vera leaf (UNII: ZY81Z83H0X) alcohol (UNII: 3K9958V90M) methylparaben (UNII: A2I8C7HI9T) mineral oil (UNII: T5L8T28FGP) paraffin (UNII: I9O0E3H2ZE) propylparaben (UNII: Z8IX2SC1OH) water (UNII: 059QF0KO0R) petrolatum (UNII: 4T6H12BN9U) white wax (UNII: 7G1J5DA97F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0924-5701-05 12 in 1 BOX 1 NDC:0924-5701-01 0.9 g in 1 PACKET 2 NDC:0924-5701-06 25 in 1 BOX 2 NDC:0924-5701-01 0.9 g in 1 PACKET 3 NDC:0924-5701-07 60 in 1 BOX 3 NDC:0924-5701-01 0.9 g in 1 PACKET 4 NDC:0924-5701-08 144 in 1 BOX 4 NDC:0924-5701-01 0.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/27/2012 Labeler - Acme United Corporation (001180207) Registrant - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 MANUFACTURE(0924-5701)