Drug Facts

Active ingredients	Purpose
Pramoxine HCl 1.0% (w/w)	External Analgesic
Zinc Acetate 0.12 % (w/w)	Skin Protectant

Uses

for the temporary relief of pain and itching associated with poison ivy, poison oak, poison sumac, insect bites or minor skin irritations.
dries the oozing and weeping of poison:
- ivy
- oak
- sumac

Warnings

For external use only

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

do not use more often than directed.
as soon as possible after exposure, wash affected area with soap and water. Gently pat dry.
apply Ivarest Poison Ivy Itch Spray liberally.
wash hands after use.
adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily.
children under 2 years of age: consult a doctor.

glycerin, PEG-40 hydrogenated castor oil, phenoxyethanol, propylene glycol, purified water, SD alcohol 38-B, sodium citrate

Quick Relief Spray

MAXIMUM STRENGTH
IVAREST®
EXTERNAL ANALGESIC/SKIN PROTECTANT

POISON IVY
ITCH SPRAY

Also Great For
Insect Bites!

No Rub,
No Mess
Stays Where You Spray It
To Protect Affected Area

Soothes
Skin Fast
Relieves Itch and Pain,
Comforts Irritated Skin

Poison Ivy, Oak & Sumac,
Insect Bites, Minor Skin Irritations

Net 3.4 fl oz. (100 mL)

BLISTEX IVAREST POISON IVY ITCH
zinc acetate and pramoxine hydrochloride spray

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Zinc Acetate (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	Zinc Acetate	0.12 g in 100 mL
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
Propylene Glycol (UNII: 6DC9Q167V3)
Glycerin (UNII: PDC6A3C0OX)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
Phenoxyethanol (UNII: HIE492ZZ3T)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10157-2100-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/02/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part347	02/02/2015

Labeler - Blistex Inc. (005126354)

Name	Address	ID/FEI	Business Operations
Establishment
Blistex Inc.		005126354	MANUFACTURE(10157-2100)