41163-816 SuperValu Equaline IPA prep pads

Manufacturer
SuperValu, Inc. | Medline Industries, LP
Effective date
2026-09-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-09-08 02:02:45

Label at a glance#

ProductAlcohol
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Dosage and administration

clean the affected area discard after a single use may be covered with a sterile bandage

Storage and handling

do not flush protect from freezing and avoid excessive heat not made with natural rubber latex

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

  • first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • do not get in the eyes or apply over large areas of the body
  • in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
  • do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor

OTC - STOP USE SECTION

if the condition persists or gets worse

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

  • clean the affected area
  • discard after a single use
  • may be covered with a sterile bandage

Other information

STORAGE AND HANDLING SECTION

  • do not flush
  • protect from freezing and avoid excessive heat
  • not made with natural rubber latex

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Manufacturing Information

SPL UNCLASSIFIED SECTION

Distributed by UNFI

Providence, RI 02903 USA

Packaged in China with components from Taiwan

REF: EQU090734R

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eacheachBoxBox

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041163263345GTIN-13: 0041163263345
EAN-13: 0041163263345
GTIN-12: 041163263345
UPC-A: 041163263345
GTIN storage (14 digits): 00041163263345
41163-816-30 Box.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41163-816-30EA - Each41163-816b751b9ea-1a39-4ebe-b2fd-c2194ac81b1212024-04-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163023
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163023
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-81641163-816-30

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
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72025-01-03full-release2026-06-01 00:50:40

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
AlcoholISOPROPYL ALCOHOLSuperValu, Inc.5e6e6d6f-4472-40f1-b0a9-96cee7ef075b2026-09-04WarningsExact identifier
ndc (package): 41163-816-30
ndc (product): 41163-816
ndc11 (package): 41163081630
spl id: 5aaecb69-42f2-288b-e063-6394a90a48a2
spl set id: 5e6e6d6f-4472-40f1-b0a9-96cee7ef075b

Reported adverse events (FAERS/openFDA)#

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