ITCH RELIEF- diphenhydramine hcl and zinc acetate spray

Itch Relief by

Drug Labeling and Warnings

Itch Relief by is a Otc medication manufactured, distributed, or labeled by FSA Store Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Diphenhydramine HCl 2.0%,

​Purpose

External analgesic

​Uses

for the temporary relief of pain and itching associated with:

• minor burns
• minor cuts
• scrapes
• insect bites
• minor skin irritations

Warnings

For external use only.

Flammable:

Keep away from fire or flame.

​Do not use

• on large areas of the body
• on chicken pox, poison ivy, or sunburn
• on broken, blistered, or oozing skin
• more often than directed
• with any other product containing diphenhydramine, even one taken by mouth

​When using this product

• avoid contact with the eyes

​Stop use and ask doctor if

• conditions worsens
• symptoms persist for 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

• adults and children 2 years of age and older: spray on affected area not more than 3 to 4 times daily.
• children under 2 years of age: do not use, consult a doctor.

​Other information

• store between 20° to 25°C (68° to 77°F)
• shake well before use
• pump must be primed before use

​ ​Inactive ingredients

SD ALCOHOL 40-B, WATER, GLYCERIN, CAMPHOR, TROMETHAMINE, PVP, ALOE BARBADENSIS LEAF JUICE

​Questions?

1-866-964-0939

​Principal Display Panel

caring mill

Extra Strength

Itch Relief

Pump Spray

Diphenhydramine Hydrochloride 2%/

External Analgesic

Easy-To-Spray Pump

• Relieves pain and itching associated

with minor burns, cuts, scrapes,

insect bites, and skin irritations

• Helps cool & soothe skin
• Ozone-Friendly, Non-Aerosol

2.5 FL. OZ. (74 mL)

INGREDIENTS AND APPEARANCE

ITCH RELIEF 
diphenhydramine hcl and zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81522-726
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
TROMETHAMINE (UNII: 023C2WHX2V)
PVP (UNII: FZ989GH94E)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81522-726-01	74 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/19/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/19/2025

Labeler - FSA Store Inc. (049283340)