FDA Label for Quality Choice Itch Relief
View Indications, Usage & Precautions
Quality Choice Itch Relief Product Label
The following document was submitted to the FDA by the labeler of this product Chain Drug Marketing Association. 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 Ingredient
Diphenhydramine hydrochloride 2% Topical analgesic
Zinc acetate 0.1% Skin protectant
Uses
for
temporary relieves pain and itching due to:
insect bites
minor burns
sunburn
minor skin irritations
minor cuts
scrapes
rashes due to poison ivy, poison oak, and poison sumac
dries the oozing and weeping of poison:
ivy
oak
sumac
Directions
do not use more often than directed
adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily
children under 2 years: ask a doctor
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 Doctor Before Use
on chicken pox
on measles
When Using This Product
do not get into eyes
Stop Use And Ask Physician
condition worsens
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.
Warning
for external use only
Purposes
Itch relief
Inactive Ingredients
Purified Water, Glycerin, SD Alcohol, Povidone, Povidonee (K-30), Trolamine
Prinicpal Dispaly Panel
Quality Choice
Compare to the active ingredients in BENADRYL® ITCH RELIEF SPRAY
Extra Strength Itch Relief Spray
Skin protectant Topical analgesic
Diphenhydramine hydrochloride 2% Zinc acetate 0.1%
For Skin Use Only
* Please review the disclaimer below.
