FDA.reportPublic FDA data

Sentry Anti-Itch Spray

Manufacturer
Sergeant's Pet Care Products LLC | Diversified Manufacturing Corporation
Effective date
2021-11-10
Label type
OTC ANIMAL DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:28:24

Label at a glance#

ProductSentry Anti-Itch
Active ingredientBENZYL ALCOHOL, BENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

SHAKE WELL BEFORE USE. Hold spray 6-8 inches from affected area and apply liberally. Use as often as necessary for continued relief. Discontinue use should symptoms persist, consult a veterinarian.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Sentry Anti-Itch Spray for dogs Itch Relief Soothes dry skin irritationsSkin irritationsAllergy dermatitisContains Witch Hazel Soothing Anti-Itch Formula

OTC - PURPOSE SECTION

SENTRY Anti-itch Spray for dogs was clinically developed and tested by a veterinary dermatologist for aiding the soothing, drying and healing of moist "hot spot." It also relieves itching and helps control the spread of lesions. Provides immediate soothing relief. Does not sting on application. Safe for dogs at least 6 weeks of age.

DIRECTIONS FOR USE:

DOSAGE & ADMINISTRATION SECTION

SHAKE WELL BEFORE USE. Hold spray 6-8 inches from affected area and apply liberally. Use as often as necessary for continued relief. Discontinue use should symptoms persist, consult a veterinarian.

PRECAUTION:

PRECAUTIONS SECTION

For Animal Use Only. FOR EXTERNAL USE ONLY. Avoid contact with eyes or mucus membranes. In case of contact, flush eyes with water and seek medical attention if irritation persists.

WARNING:

WARNINGS SECTION

Wash hands after use. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.05% w/w, Benzyl Alcohol 2% w/w

OTHER INGREDIENTS:

INACTIVE INGREDIENT SECTION

Allantoin, FD&C Blue #1, Hamamelis Virginiana Water (Witch Hazel), Propylene Glycol, Purified Water, Sucrose Octaacetate (helps reduce wound biting)

STORAGE AND HANDLING SECTION

Store at room temperature.

HOW SUPPLIED

HOW SUPPLIED SECTION

8.4 FL OZ (248 mL)

P002667-5 AMIA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZYL ALCOHOLACTIVE INGREDIENTLKG8494WBH1
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
BENZYL ALCOHOLACTIVE MOIETYLKG8494WBH1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21091-11021091-110-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Zilactin Early Relief Cold SoreBENZYL ALCOHOLASCENT CONSUMER PRODUCTS, INC42ef8bfa-c4d9-01cf-e063-6394a90ac88a2025-11-06WarningsName fallback
generic name: BENZYL ALCOHOL

Reported adverse events (FAERS/openFDA)#

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