Quality Choice Extra Strength Itch Relief Spray

Manufacturer: Chain Drug Marketing Association | Weeks & LEO, Inc. | Weeks & Leo
Effective date: 2025-11-12
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:43:35

Label at a glance#

ProductQuality Choice Itch Relief

Active ingredientZINC ACETATE, DIPHENHYDRAMINE HYDROCHLORIDE

Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

INDICATIONS & USAGE SECTION

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 & ADMINISTRATION SECTION

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 AND PRECAUTIONS SECTION

For external use only

OTC - DO NOT USE SECTION

on large areas of the body

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

OTC - ASK DOCTOR SECTION

on chicken pox

on measles

OTC - WHEN USING SECTION

do not get into eyes

OTC - STOP USE SECTION

condition worsens

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Warning

WARNINGS SECTION

for external use only

OTC - PURPOSE SECTION

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Back LabelQC spray two Ounces .jpg

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

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1053138	diphenhydrAMINE/Zinc acetate (Topical)	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1053138	diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray	PSN	5
1053138	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray	SCD	5
1053138	diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray	SY	5

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
DIPHENHYDRAMINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813
ZINC CATION Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0635515970328	GTIN-13: 0635515970328 EAN-13: 0635515970328 GTIN-12: 635515970328 UPC-A: 635515970328 GTIN storage (14 digits): 00635515970328	05-259v2.0 QC Back label Itch Spray .jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63868-952-02	Quality Choice Itch Relief	59 mL in 1 BOTTLE, SPRAY	SPRAY	59		5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

Quality Choice Itch Relief
Diphenhydramine HCl, Zinc Acetate
WATER
GLYCERIN
ALCOHOL
POVIDONE K30
TROLAMINE
ZINC ACETATE
ZINC CATION
DIPHENHYDRAMINE HYDROCHLORIDE
DIPHENHYDRAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63868-952	63868-952-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	IACT
POVIDONE K30	U725QWY32X	IACT
TROLAMINE	9O3K93S3TK	IACT
ZINC ACETATE	FM5526K07A	ACTIB
DIPHENHYDRAMINE HYDROCHLORIDE	TC2D6JAD40	ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
4	2019-04-23	full-release	2026-05-31 22:59:19

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Quality Choice Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Chain Drug Marketing Association	8735b298-83f3-0b5d-e053-2a91aa0a8292	2025-11-12	Warnings	Exact identifier ndc (package): 63868-952-02 ndc (product): 63868-952 ndc11 (package): 63868095202 spl id: 436a3341-6fa3-f535-e063-6294a90aeba4 spl set id: 8735b298-83f3-0b5d-e053-2a91aa0a8292

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.