Quality Choice Extra Strength Itch Relief Spray

Quality Choice Extra Strength Itch Relief Spray
SPL v5
SPL
SPL Set ID 8735b298-83f3-0b5d-e053-2a91aa0a8292
Route
TOPICAL
Published
Effective Date 2014-04-14
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Zinc Cation (0.1 g) Diphenhydramine (2 g)
Inactive Ingredients
Water Glycerin Alcohol Povidone K30 Trolamine

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2014-04-14

Description

Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant


Medication Information

Indications and Usage

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

Dosage and Administration

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

Description

Diphenhydramine hydrochloride 2% Topical analgesic Zinc acetate 0.1% Skin protectant

Section 43685-7

For external use only

Section 50565-1

If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9

condition worsens

symptoms last more than 7 days or clear up and occur again within a few days

Section 50567-7

do not get into eyes

Section 50569-3

on chicken pox

on measles

Section 50570-1

on large areas of the body

with any other product containing diphenhydramine, even one taken by mouth

Section 51727-6

Purified Water, Glycerin, SD Alcohol, Povidone, Povidonee (K-30), Trolamine

Section 51945-4

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

Section 55105-1

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

Section 55106-9

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

Warning

for external use only


Structured Label Content

Indications and Usage (34067-9)

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

Dosage and Administration (34068-7)

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

Section 43685-7 (43685-7)

For external use only

Section 50565-1 (50565-1)

If swallowed, get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

condition worsens

symptoms last more than 7 days or clear up and occur again within a few days

Section 50567-7 (50567-7)

do not get into eyes

Section 50569-3 (50569-3)

on chicken pox

on measles

Section 50570-1 (50570-1)

on large areas of the body

with any other product containing diphenhydramine, even one taken by mouth

Section 51727-6 (51727-6)

Purified Water, Glycerin, SD Alcohol, Povidone, Povidonee (K-30), Trolamine

Section 51945-4 (51945-4)

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

Section 55105-1 (55105-1)

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

Section 55106-9 (55106-9)

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

Warning

for external use only


Advanced Ingredient Data


Raw Label Data

All Sections (JSON)