OTC Medication Information: Itch Relief

ITCH RELIEF- diphenhydramine hydrochloride and zinc acetate spray
OLD EAST MAIN CO

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

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 in eyes

Stop use and ask a doctor if

condition worses 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 to 25⁰ C (68⁰ to 77⁰ F)

Inactive ingredients

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

*Not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Benadryl Spray

DISTRIBUTED BY ONE EAST MAIN CO.

100 MISSION RIDE

GOODLETTSVILLE, TN 37072

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TEAR HERE

DG health

Compare to active ingredents in Benadryl Spray

Itch Relief Spray

External Analgesic

Skin Protectant

Relieves itching due to insect bites, poison oak or ivy, or other monor skin irritations

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2 FL OZ (59 mL)

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ITCH RELIEF
diphenhydramine hcl, zinc acetate spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-295
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 20 mg in 1 mL
ZINC ACETATE (ZINC CATION) ZINC ACETATE 1 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
GLYCERIN
POVIDONE
WATER
TROMETHAMINE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55910-295-20 59 mL in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 07/14/2010
Labeler — OLD EAST MAIN CO (068331990)
Registrant — Vi-Jon, LLC (790752542)
Establishment
Name Address ID/FEI Operations
Vi-Jon, LLC 790752542 manufacture (55910-295)
Establishment
Name Address ID/FEI Operations
Vi-Jon, LLC 088520668 manufacture (55910-295)

Revised: 10/2023 OLD EAST MAIN CO

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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