Bite&Sting Relief Spray [GNP]

Bite and Sting Relief by

Drug Labeling and Warnings

Bite and Sting Relief by is a Otc medication manufactured, distributed, or labeled by Amerisource Bergen LLC, Inspec Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BITE AND STING RELIEF GNP- benzocaine spray 
Amerisource Bergen LLC

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Bite&Sting Relief Spray [GNP]

Active ingredient                                       Purpose

Benzocaine 5.0% ....................................... Pain Relief

Uses

For the temporary relief of pain and itching associated with insect bites.

Warnings
For external use only.

Flammable:Do not use while smoking or near heat or flame
When using this product avoid contact with the eyes use only as directed. do not puncture or incinerate.

Contents under pressure.
Do not store at temperatures above 120°F.

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of the reach of children.

 In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

 shake well Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Ask a doctor.

Inactive ingredients

Aloe Barbadensis Leaf Juice Extract, Ascorbic Acid, Camphor, Chamomilla Recutita (Matricaria) Flower, Extract, Cholecalciferol, Diisopropyl Adipate, Eugenia Caryophyllus (Clove) Flower Oil, Fragrance, Mentha Piperita ( Peppermint) Oil, Octyldodecanol, Olea Europaea (Olive) Fruit Oil,

PE -8 Dimethicone, Propylene lycol, Pyridoxine HCI, Retinyl Palmitate, SD Alcohol 40, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica, 

Tocopheryl Acetate, Zea Mays (Corn) Oil.

Questions?

888-793-8450

BITE AND STING RELIEF  GNP
benzocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46122-653
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORN OIL (UNII: 8470G57WFM)
ALOE ARBORESCENS FLOWER (UNII: U449SE7IPV)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
MATRICARIA CHAMOMILLA LEAF (UNII: 6I9LN466F0)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
CLOVE OIL (UNII: 578389D6D0)
PEPPERMINT OIL (UNII: AV092KU4JH)
OCTYLDODECANOL (UNII: 461N1O614Y)
OLIVE OIL (UNII: 6UYK2W1W1E)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALCOHOL (UNII: 3K9958V90M)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46122-653-34	85 g in 1 PACKAGE; Type 0: Not a Combination Product	01/18/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	01/18/2021	12/09/2025

Labeler - Amerisource Bergen LLC (007914906)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC		081030372	manufacture(46122-653)

Revised: 12/2025

Document Id: 4585cac3-ec09-8c66-e063-6294a90a8706

34390-5

Set id: 3c9689cc-f597-4337-a45c-632959d357dc

Version: 5

Effective Time: 20251209