Itch Relief Spray
FDA Label NDC 70000-0023

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health, 110 Dba Leader for the product Itch Relief (NDC 70000-0023). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, flammable, do not use, ask a doctor before use, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Diphenhydramine HCl 2%
Zinc Acetate 0.1%

Purpose

External analgesic
Skin protectant

Uses

  • for the temporary relief of pain and itching associated with minor skin irritations
  • dries the oozing and weeping of poison: ivy, oak, sumac

Warnings

For external use only

Flammable

Keep away from fire of flame.

Do Not Use

  • on large areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask A Doctor Before Use

on chicken pox or measles

When Using This Product

do not get into eyes

Stop Use And Ask A Doctor If

condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • do not use more than directed
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

Other Information

• store at 20⁰ - 25⁰C (68⁰ - 77⁰F)

Inactive Ingredients

alcohol, glycerin, povidone, purified water, tris (hydroxymethyl)aminomethane

Questions & Comments?

1-800-593-0593

Adverse Reactions

Dist. by CAH, Dublin, OH 43017

2019 Cardinal Health

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company of the registered trademark Benadryl Extra Strength Spray.

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NDC 70000-0023-1

Extra Strength

Itch Relief Spray

Diphenhydramine HCI, 2% Zinck Acetate, 0.1%

External Analgesic

Skin Protectant

COMPARE TO BENADRYL EXTRA STRENGTH SPRAY

active ingredients

100% Money Back Guarantee

Relieves Itching

Due to Insect Bits,

Poison Oak or Ivy, or Other Minor Skin Irritations

2 FL OZ (59 mL)

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