CHIGG AWAY- benzocaine lotion 
Humco Holding Group, Inc.

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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Private Label Chigg Away

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.

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

Inactive Ingredient

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

CVS

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

HEBChigg.jpg

CHIGG AWAY 
benzocaine lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-9105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0395-9105-94118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884analysis(0395-9105) , manufacture(0395-9105) , pack(0395-9105) , label(0395-9105)

Revised: 6/2020
Document Id: a877a829-31fe-424f-e053-2995a90a2822
Set id: 605106c9-354f-2733-e053-2a91aa0a94f6
Version: 3
Effective Time: 20200619
 
Humco Holding Group, Inc.