FDA.reportPublic FDA data

Signature Select Pain Relieving Spray 5 oz

Manufacturer
Safeway/Albartsons | Nantong Health & Beyond Hygienic Products Inc
Effective date
2025-10-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:39:18

Label at a glance#

ProductSignature Select Pain Relieving
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Label structure13 sections

Indications and uses

First aid to help prevent bacterial contamination or skin infection and for temporary relief of pain and itching associated with ■ minor burns ■ sunburn ■ minor cuts ■scrapes ■ insect bites ■ minor skin irritations

Dosage and administration

■Adults and children 2 years and older: Cleananddry affectedarea. Shake well;spray small amount on the area 1 to 3 times daily. May be covered witha sterilebandage;let dry first. ■ Children under 2 years af age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients 

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Cl 0.13% 

LidocaineHCI 4%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic 
Pain relieving 

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent bacterial contamination or skin infection and for temporary relief of pain and itching associated with

■ minor burns

■ sunburn

■ minor cuts

■scrapes

■ insect bites

■ minor skin irritations

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

■ avoid contact w th eyes

■ do not use in large quantities, particularly over raw surfaces or blistered areas

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

■deep or puncture wounds

■ animalbites

■ serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens

■ symptoms persist for more than 7 days

■symptoms clear up and occur again w thin a few days

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center (1-800-222-1222) right away.

Directions 

DOSAGE & ADMINISTRATION SECTION

■Adults and children 2 years and older: Cleananddry affectedarea. Shake well;spray small amount on the area 1 to 3 times daily.
May be covered witha sterilebandage;let dry first.

■ Children under 2 years af age: ask a doctor

Other information

OTHER SAFETY INFORMATION

Avoid excessive heat

Inactive Ingredients

INACTIVE INGREDIENT SECTION

disodium EDTA, melaleuca alterniflia (tea Tree) leaf oil, octoxynol-9, propylene glycol, water

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-866-1313

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2047877benzalkonium chloride 0.13 % / lidocaine HCl 4 % Topical SprayPSN2
2047877benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 40 MG/ML Topical SpraySCD2
2047877benzalkonium chloride 0.13 % / lidocaine HCl 4 % Topical SpraySY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-931-01Signature Select Pain Relieving148 mL in 1 BOTTLE, SPRAYSPRAY1482

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21130-93121130-931-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
OCTOXYNOL 97JPC6Y25QSIACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR

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
Signature Select Pain RelievingLIDOCAINE HCL, BENZALKONIUM CHLORIDESafeway/Albartsons3cab1b0c-4ffd-9c01-e063-6294a90ad15d2025-10-16WarningsExact identifier
ndc (package): 21130-931-01
ndc (product): 21130-931
ndc11 (package): 21130093101
spl id: 414a1a11-867c-10c1-e063-6394a90a39a4
spl set id: 3cab1b0c-4ffd-9c01-e063-6294a90ad15d

Reported adverse events (FAERS/openFDA)#

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