37808-809 HEB alcohol prep pad

Manufacturer
H-E-B | Medline Industries, LP
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
daily-update
Hydrated at
2026-08-22 01:01:30

Label at a glance#

ProductinControl alcohol
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:
H-E-B

646 S Flores St, San Antonio, TX 78204 USA

Packaged in China with components from Taiwan

REF: HEB090731CV1

V2 RJ23LPD

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EachEachBoxBox

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

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
37808-80937808-809-30, 37808-809-60, 37808-809-09

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
82025-01-03full-release2026-06-01 00:50:39

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
inControl alcoholISOPROPYL ALCOHOLH-E-B45dfbd7a-0ae1-4146-9527-5483c884e6362026-08-18WarningsExact identifier
ndc (package): 37808-809-60
ndc (package): 37808-809-30
ndc (package): 37808-809-09
ndc (product): 37808-809
ndc11 (package): 37808080930
ndc11 (package): 37808080960
ndc11 (package): 37808080909
spl id: 59568b8e-d818-2183-e063-6294a90a6100
spl set id: 45dfbd7a-0ae1-4146-9527-5483c884e636

Reported adverse events (FAERS/openFDA)#

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