FDA.reportPublic FDA data

Up and Up Max Pain Relieving Cleansing Spray

Manufacturer
TARGET CORPORATION
Effective date
2025-01-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:53:22

Label at a glance#

ProductUp and Up Max Pain Relieving Cleansing
Active ingredientBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Label structure12 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: cuts scrapes burns sunburn skin irritations

Dosage and administration

adults and children 2 years and older: clean the affected area spray a small amount on the area 1-3 times daily may be covered with a sterile bandage if bandaged, let dry first children under 2 years of age: do not use, consult a doctor

Storage and handling

avoid excessive heat store at room temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Cl 0.13%
Lidocaine HCl 4.0%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic
Pain relieving spray

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:

  • cuts
  • scrapes
  • burns
  • sunburn
  • skin irritations

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • do not use in or near the eyes
  • do not apply over large areas of the body or in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older:
  • clean the affected area
  • spray a small amount on the area 1-3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first
  • children under 2 years of age: do not use, consult a doctor

Other information

STORAGE AND HANDLING SECTION

  • avoid excessive heat
  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol, disodium EDTA, fragrances, propylene glycol, purified water, sodium hydroxide

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82941E1F182941E1F1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2047877benzalkonium chloride 0.13 % / lidocaine HCl 4 % Topical SprayPSN1
2047877benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 40 MG/ML Topical SpraySCD1
2047877benzalkonium chloride 0.13 % / lidocaine HCl 4 % Topical SpraySY1

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
82442-018-21Up and Up Max Pain Relieving Cleansing150 mL in 1 BOTTLELIQUID1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-018UP AND UP MAX PAIN RELIEVING CLEANSING (BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE) LIQUID [TARGET CORPORATION]1Current NDC, 1 package rows20250123_2c3e72eb-5d98-1f3f-e063-6394a90ab00c.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-01882442-018-21

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
NameUNIIKind
ALCOHOL3K9958V90MIACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE DISODIUM7FLD91C86KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
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
Up and Up Max Pain Relieving CleansingBENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDETARGET CORPORATION2c3e72eb-5d98-1f3f-e063-6394a90ab00c2025-01-21WarningsExact identifier
ndc (package): 82442-018-21
ndc (product): 82442-018
ndc11 (package): 82442001821
spl id: 2c3e8149-f59a-4b05-e063-6394a90ad10b
spl set id: 2c3e72eb-5d98-1f3f-e063-6394a90ab00c

Reported adverse events (FAERS/openFDA)#

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