FIRST AID AND BURN- benzalkonium chloride, lidocaine hydrochloride cream 
Safetec of America, Inc.

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61010-5701, First Aid and Burn Cream

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Lidocaine HCl 0.5%

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

Warnings

For external use only

Do not use

  • in eyes
  • in large quantities
  • over raw or blistered areas, or on deep puncture wounds, animal bites, serious burns
  • for more than one week unless directed by a doctor

Keep out of reach of children.

If ingested contact a Poison Control Center right away.

Directions

Inactive ingredients

aloe vera, emulsifying wax, ethyl alcohol, methylparaben, mineral oil, paraffin, propylparaben, purified water, white petrolatum, white wax

PRINCIPAL DISPLAY PANEL – 0.9 gram packet

NDC 61010-5701-03

Safetec

First Aid &
Burn Cream

0.9 g (1/32 oz.)

Safetec of America, Inc.
Buffalo, NY 14215
800-456-7077

PRINCIPAL DISPLAY PANEL – 0.9 gram packet

PRINCIPAL DISPLAY PANEL – 144 count box

NDC 61010-5701-4

Safetec

First Aid

First Aid & Burn Cream

Reorder No. 53410
To reorder:
Call: 1-800-456-7077
Fax: 716-895-2969
Online: www.safetec.com

PRINCIPAL DISPLAY PANEL –  144 count box

Principal Display Panel – 10 Packet Box Label

Safetec ®

FIRST AID

Burn Cream

Quickly soothes pain caused by minor burns
and protects against infection

10 Packets

Each Packet Net. Wt. 0.9g

Made in USA

Reorder No. 53408

Principal Display Panel – 10 Packet Box Label
FIRST AID AND BURN 
benzalkonium chloride, lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61010-5701
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61010-5701-4144 in 1 BOX09/21/2012
1NDC:61010-5701-30.9 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:61010-5701-525 in 1 BOX09/21/2012
2NDC:61010-5701-30.9 g in 1 PACKET; Type 0: Not a Combination Product
3NDC:61010-5701-610 in 1 BOX04/01/2020
3NDC:61010-5701-30.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00309/21/2012
Labeler - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262manufacture(61010-5701)

Revised: 2/2024
Document Id: 10d3fc91-82a0-e8eb-e063-6394a90ae87b
Set id: 47cb6921-5d82-4123-a9e0-0b05d4dcb5b2
Version: 5
Effective Time: 20240207
 
Safetec of America, Inc.