BITE AND STING MEDICATED RELIEF PADS CVS- benzocaine - 5.00% liquid

Bite and Sting Medicated Relief Pads by

Drug Labeling and Warnings

Bite and Sting Medicated Relief Pads by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                   Purpose

Benzocaine - 5.00%                Pain Relief

PURPOSE

Uses

For temporarily relief of pain and itching associated with minor cuts, scrapes and minor burns

WarningsFor external use only

Flammable: ​ do not use while smoking or near heat or flame

When using this product

• avoid contact with eyes
• use only as directed

Stop use and ask a doctor if

condition worsens
symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children
In case of accidental ingestion, seek professional or contact a Poison Control Center immediately.

Direction

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, 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,
PEG-8 Dimethicone, Propylene Glycol, Pyridoxine HCl, Retinyl Palmitate, SD Alcohol 40, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica,
Tocopheryl Acetate, Zea Mays (Corn) Oil

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BITE AND STING MEDICATED RELIEF PADS  CVS
benzocaine - 5.00% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-856
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
CHAMOMILE (UNII: FGL3685T2X)
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)
Sodium Propoxyhydroxypropyl Thiosulfate Silica (UNII: 208G222332)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORN OIL (UNII: 8470G57WFM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-856-03	72 g in 1 JAR; Type 0: Not a Combination Product	04/15/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/15/2017

Labeler - CVS (062312574)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(69842-856) , label(69842-856)