CVS ITCH RELIEF AND REPELLENT- benzocaine lotion

CVS Itch Relief and Repellent by

Drug Labeling and Warnings

CVS Itch Relief and Repellent by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Humco Holding Group, inc., Humco Holding Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

CVS Itch Relief & Repellent

Drug Facts

Active Ingredient

Benzocaine 5%

Purpose

Anesthetic

Use

Relieves itching and discomfort due to nonpoisonous insect bites such as chiggers (redbugs), mosquitoes, ticks, fleas, no-see-ums, biting flies, fire ants, bees and wasps; summer’s itch.

Warnings

For external use only. Keep away from eyes or other mucous membranes. Not for prolonged use. For use on intact skin only. Do not use on children younger than 2 yrs.

When using this product

discontinue use if the condition persists or if a rash or irritation develops and consult a doctor. As with all pesticides/drugs,

keep out of the reach of children.

In case of accidental ingestion, contact physician or poison control center at once.

Directions: As an anti-itch.

• Adults and children 2 yrs. of age and over. Apply topically and rub well as needed.
  
• Children under 2 yrs. of age: Do not use 

As an insect (chigger) repellent: Apply around feet, ankles, waist and to skin under all areas of tight clothing and around all openings in outer clothing. Reapply after heavy perspiration.

Other Information

• Disposal: Do not reuse bottle. Rinse thoroughly before discarding.

Inactive Ingredient

Cetyl alcohol. Glycerin, Glyceryl stearate, Hydroxyethyl cellulose, Isopropyl alcohol, Methylparaben, Petrolatum, Propylparaben, Purified water, Sodium lauryl sulfate, Stearic acid, Sulfur, and Triothanolamine..

PRINCIPAL DISPLAY PANEL

Itch Relief
& Repellent
Relieves itching & Repels
Chiggers ( Redbugs)
4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

CVS ITCH RELIEF AND REPELLENT 
benzocaine lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-167
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYLPARABEN (UNII: A2I8C7HI9T)
PETROLATUM (UNII: 4T6H12BN9U)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
STEARIC ACID (UNII: 4ELV7Z65AP)
SULFUR (UNII: 70FD1KFU70)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-167-94	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	01/01/2008

Labeler - CVS Pharmacy (062312574)

Registrant - Humco Holding Group, inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	analysis(69842-167) , manufacture(69842-167) , pack(69842-167) , label(69842-167)