PAIN RELIEF ALCOHOL SWABS- benzocaine swab

Pain Relief Alcohol Swabs by

Drug Labeling and Warnings

Pain Relief Alcohol Swabs by is a Otc medication manufactured, distributed, or labeled by Amerisource Bergen. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Benzocaine 6%
Isopropyl alcohol 70% v/v

PURPOSE

Topical Anesthetic

Antiseptic

USES

• For preparation of the skin prior to injection
• For temporary relief of pain and itching associated with minor burns, sunburn, minor skin irritations, or insect bites

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.

SPL UNCLASSIFIED SECTION

OTHER INFORMATION

Store at room temperature: 15° - 30° C (59° - 86° F)

INACTIVE INGREDIENTS

propylene glycol, purified water

QUESTIONS

CARTON INFORMATION

NDC: 124385-982-41

GOOD NEIGHBOR PHARMACY

Pain Relief Alcohol Swabs
with Benzocaine

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

80 Individually Wrapped Foil Packets


Distributed by
AmerisourceBergen
Valley Forge, PA 19482-0959

Visit us at www.myGNP.com

INGREDIENTS AND APPEARANCE

PAIN RELIEF ALCOHOL SWABS 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24385-982
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzocaine (UNII: U3RSY48JW5) (benzocaine - UNII:U3RSY48JW5)	benzocaine	0.06 mL
isopropyl alcohol (UNII: ND2M416302) (isopropyl alcohol - UNII:ND2M416302)	isopropyl alcohol	0.70 mL

Inactive Ingredients
Ingredient Name	Strength
propylene glycol (UNII: 6DC9Q167V3)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24385-982-41	80 in 1 CARTON
1		1 in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/01/2007

Labeler - Amerisource Bergen (007914906)