CHIGG AWAY- benzocaine lotion

Chigg Away by

Drug Labeling and Warnings

Chigg Away by is a Otc medication manufactured, distributed, or labeled by Westlake HB Pharma LLC, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Chigg Away

Drug Facts

Active Ingredient

Benzocaine 5%

Purpose

Anesthetic

Uses

Relieves itching and discomfort due to nonpoisonous insect bites such as chiggers (redbugs), mosquitoes, ticks, and fleas, no-see-ums, biting flies, fire ants, bees and wasps; swimmers 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 rash or irritation develops and consult a doctor. As with all pesticides/drugs,

keep out of reach of children.

In case of accidental ingestion, contact a 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 years 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 respiration.

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, Triethanolamine..

PRINCIPAL DISPLAY PANEL

NDC: 86000-857-05

CHIGG

STOP

RELIEVES ITCHING

REPELS CHIGGERS

4 FL OZ

(118 ML)

INGREDIENTS AND APPEARANCE

CHIGG AWAY 
benzocaine lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82895-857
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)
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)
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82895-857-05	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/23/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/23/2022

Labeler - Westlake HB Pharma LLC (081176855)

Registrant - Pharma Nobis, LLC (118564114)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	analysis(82895-857) , pack(82895-857) , manufacture(82895-857) , label(82895-857)