ALCOHOL PREP PADS WITH PAIN RELIEF - benzocaine swab 
McKesson

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.

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DRUG FACTS

ACTIVE INGREDIENTS

Benzocaine 6%
Isopropyl alcohol 70% v/v

PURPOSE

Topical Anesthetic

Antiseptic

USES

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

Do not use

  • in the eyes
  • with electrocautery procedures




Stop use and ask a doctor

  • if irritation and redness develop
  • if symptoms persist for more than 72 hours or symptoms clear up and occur within a few days.


Ask a doctor or pharmacist

if you are pregnant or nursing a baby.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Prior to Injection - Adults and children 2 years of age or older:
Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.

Insect bites, skin irritations, minor burns, sunburn -
Adults and children 2 years of age or older:

Apply to the affected site not more than 3 to 4 times daily.

Children under 2 years of age: Ask a doctor.


OTHER INFORMATION

INACTIVE INGREDIENTS

propylene glycol, water


CARTON INFORMATION

sunmark®

NDC 49348-897-39

alcohol prep pads

Antiseptic / Anesthetic
Safe and easy to use
Isopropyl Alcohol 70%

WITH BENZOCAINE FOR PAIN RELIEF

80 INDIVIDUALLY WRAPPED FOIL PACKETS


Another Quality Product Distributed by McKesson
One Post Street, San Francisco, CA 94104
Money Back Guarantee

Visit us at www.sunmarkbrand.com

CARTON

ALCOHOL PREP PADS WITH PAIN RELIEF 
benzocaine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-897
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5) benzocaine0.06 mL
isopropyl alcohol (UNII: ND2M416302) (isopropyl alcohol - UNII:ND2M416302) isopropyl alcohol0.70 mL
Inactive Ingredients
Ingredient NameStrength
propylene glycol (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-897-3980 in 1 CARTON
11 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/19/2010
Labeler - McKesson (177667227)

Revised: 9/2010
Document Id: 6c17c3de-00b9-4f92-aa3e-ec48fc7220db
Set id: cfd200b6-0a38-4d86-b8a6-ef2c9ac9102c
Version: 1
Effective Time: 20100919
 
McKesson