Label: BLISTEX IVAREST POISON IVY ITCH- zinc acetate and pramoxine hydrochloride spray
- NDC Code(s): 10157-2100-1
- Packager: Blistex Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
- 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.
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton
Quick Relief Spray
MAXIMUM STRENGTH
IVAREST®
EXTERNAL ANALGESIC/SKIN PROTECTANTPOISON IVY
ITCH SPRAYAlso Great For
Insect Bites!No Rub,
No Mess
Stays Where You Spray It
To Protect Affected AreaSoothes
Skin Fast
Relieves Itch and Pain,
Comforts Irritated SkinPoison Ivy, Oak & Sumac,
Insect Bites, Minor Skin IrritationsNet 3.4 fl oz. (100 mL)
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INGREDIENTS AND APPEARANCE
BLISTEX IVAREST POISON IVY ITCH
zinc acetate and pramoxine hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-2100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-2100-1 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 02/02/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M016 02/02/2015 Labeler - Blistex Inc. (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc. 005126354 MANUFACTURE(10157-2100)