GOOD NEIGHBOR PAIN RELIEF- benzocaine liquid

Good Neighbor Pain Relief by

Drug Labeling and Warnings

Good Neighbor Pain Relief by is a Otc medication manufactured, distributed, or labeled by AmerisourceBergen Drug Corporation (Good Neighbor Pharmacy), Lee Pharmaceuticals, AmerisourceBergen Drug Corporation, Unipack, Samson Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzocaine, 20%

Purpose

Oral anesthetic

Uses

Provides temporary relief of pain associated with the following mouth and gum irritations:

• toothache
• sore gums
• canker sores
• braces
• minor dental procedures
• dentures

Warnings

Allergy alert: Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics.

When using this product

• avoid contact with eyes
• do not exceed recommended dosage
• do not use for more than 7 days unless directed by a doctor or dentist

Stop use and ask a doctor or dentist if

• sore mouth symptoms do not improve in 7 days
• irritation, pain, or redness persists or worsens
• swelling, rash, or fever develops

Keep out of reach of children

• If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away

Directions

• Adults and children 2 years of age and older:
• wipe liquid on with cotton, or cotton swab, or finger tip.
• apply to the affected area up to 4 times daily of as directed by a doctor or dentist.
• Children under 12 years of age: adult supervision should be given in the use of this product.
• Children under 2 years of age: consult a doctor or dentist.

Inactive ingredients

Benzyl alcohol, FD&C Blue #1, FD&C Red #40, D&C yellow #10, Flavor, Methylparaben, Polyethylene Glycol, Propylene Glycol, Saccharin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOOD NEIGHBOR PAIN RELIEF 
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46122-030
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SACCHARIN (UNII: FST467XS7D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46122-030-05	1 in 1 BLISTER PACK
1	NDC: 46122-030-06	15 mL in 1 BOTTLE, GLASS

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	08/01/2008

Labeler - AmerisourceBergen Drug Corporation (Good Neighbor Pharmacy) (007914906)

Registrant - Lee Pharmaceuticals (056425432)

Establishment
Name	Address	ID/FEI	Business Operations
AmerisourceBergen Drug Corporation		007914906	label(46122-030)

Establishment
Name	Address	ID/FEI	Business Operations
Lee Pharmaceuticals		056425432	pack(46122-030)

Establishment
Name	Address	ID/FEI	Business Operations
Unipack		009248480	manufacture(46122-030)

Establishment
Name	Address	ID/FEI	Business Operations
Samson Pharmaceuticals		088169581	manufacture(46122-030)