GOODSENSE ANTI-ITCH- diphenhydramine hcl, zinc acetate spray

GoodSense Anti-Itch by

Drug Labeling and Warnings

GoodSense Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Diphenhydramine HCl 2%, Zinc Acetate 0.1%

PURPOSE

Topical Analgesic, Skin Protectant

INDICATIONS & USAGE

For the temporary relief of pain and itching associated with rashes due to poison ivy, oak and sumac, insect bites, minor skin irritations, minor cuts, dries the oozing and weeping of poison ivy, oak and sumac.

WARNINGS

Flammable. Keep away from excessive heat or open flame.

For external use only.

Do not use on chicken pox, on large areas of the body, with any other products containing diphenhydramine, even one take by mouth.

When using this product avoid spraying in eyes.

Stop use and ask a doctor if the condition worsens, rash or irritation develops and lasts for more than 7 days or clears up and occurs again within a few days.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Adults and children 2 years or older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

INACTIVE INGREDIENT

Blue 1, carbomer, isopropyl alcohol, magnesium sulfate, sodium hydroxide, water, and yellow 5.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOODSENSE ANTI-ITCH 
diphenhydramine hcl, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-064
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	2 g  in 100 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
PVP (UNII: FZ989GH94E)
TROMETHAMINE (UNII: 023C2WHX2V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-064-02	59 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/01/2025

Labeler - Geiss, Destin & Dunn, Inc (076059836)