FDA Label for Itch Relief
View Indications, Usage & Precautions
Itch Relief Product Label
The following document was submitted to the FDA by the labeler of this product Old East Main Co. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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
Other
*Not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Benadryl Spray
DISTRIBUTED BY DOLGENCORP, LLC
100 MISSION RIDE
GOODLETTSVILLE, TTN 37072
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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)
295.000/295AB
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