Label: IVAREST- zinc oxide, benzyl alcohol, and diphenhydramine hydrochloride cream
- NDC Code(s): 10157-9077-1
- Packager: Blistex Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 9, 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 (or Ivarest Poison Ivy Cleansing Foam). Gently pat dry.
- apply Ivarest liberally to form a layer you can not see through.
- 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.
- Other information
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Inactive ingredients
bentonite, benzethonium chloride, camphor, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, hydroxyethylcellulose, lanolin alcohol, lanolin oil, magnesium aluminum silicate, menthol, petrolatum, polyethylene glycol, polyglyceryl-3 diisostearate, polysorbate 60, propylene glycol, purified water, PVP, red 33, sorbitan stearate, squalane, yellow 5, yellow 6
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PRINCIPAL DISPLAY PANEL - 56 g Tube Carton
Long Lasting Cream
NDC 10157-9077-1
MAXIMUM STRENGTH
IVAREST®
EXTERNAL ANALGESIC/
POISON IVY, OAK, SUMAC DRYING CREAMPOISON IVY
ITCH CREAM8 Hour
ReliefDouble
Relief
Formula- 1
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Antihistamine
helps stop the reaction - 2
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Analgesic
soothes itch fast
Plus ... Skin protectant to help dry the rash
Poison Ivy, Oak & Sumac,
Insect Bites, Minor Skin IrritationsNet Wt. 2 oz. (56 g)
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INGREDIENTS AND APPEARANCE
IVAREST
zinc oxide, benzyl alcohol, and diphenhydramine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-9077 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 14 g in 100 g Benzyl Alcohol (UNII: LKG8494WBH) (Benzyl Alcohol - UNII:LKG8494WBH) Benzyl Alcohol 10.5 g in 100 g Diphenhydramine Hydrochloride (UNII: TC2D6JAD40) (Diphenhydramine - UNII:8GTS82S83M) Diphenhydramine Hydrochloride 2 g in 100 g Inactive Ingredients Ingredient Name Strength bentonite (UNII: A3N5ZCN45C) benzethonium chloride (UNII: PH41D05744) lanolin alcohols (UNII: 884C3FA9HE) lanolin oil (UNII: OVV5IIJ58F) magnesium aluminum silicate (UNII: 6M3P64V0NC) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) petrolatum (UNII: 4T6H12BN9U) polyethylene glycol 200 (UNII: R95B8J264J) polyglyceryl-3 diisostearate (UNII: 46P231IQV8) polysorbate 60 (UNII: CAL22UVI4M) propylene glycol (UNII: 6DC9Q167V3) water (UNII: 059QF0KO0R) D&C red no. 33 (UNII: 9DBA0SBB0L) sorbitan monostearate (UNII: NVZ4I0H58X) squalane (UNII: GW89575KF9) FD&C yellow no. 5 (UNII: I753WB2F1M) FD&C yellow no. 6 (UNII: H77VEI93A8) camphor (synthetic) (UNII: 5TJD82A1ET) povidone-iodine (UNII: 85H0HZU99M) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-9077-1 1 in 1 CARTON 12/31/2007 1 56 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 12/31/2007 Labeler - Blistex Inc (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc 005126354 MANUFACTURE(10157-9077)