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

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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Drag Facts

Active ingredient Purpose

Benzocaine - 5.00% Pain Relief

Uses

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

Warnings
For 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 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

image description

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

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

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

Labeler - CVS (062312574)

Registrant - Product Quest Mfg (927768135)

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