First Aid Kit

Manufacturer
Lami Products, Inc.
Effective date
2018-12-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:39:33

Label at a glance#

ProductFirst Aid Kit
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Preparation of the skin prior to injection.

Dosage and administration

Wipe Injection site Vigorously and discard.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isoprophyl Alcohol 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses

INSTRUCTIONS FOR USE SECTION

Preparation of the skin prior to injection.

Warnings

WARNINGS SECTION

For esternal use only.

Flammable, keep away from fire of flame.

Do not use

OTC - DO NOT USE SECTION

  • With electrocautery procedures
  • In the eyes

Stop Use

OTC - STOP USE SECTION

If irriration or redness develops.

if condition persist for more than 72 hours, consult a doctor.

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

Wipe Injection site Vigorously and discard.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70430-01070430-010-00
70430-01170430-011-00

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
7dec8140-064c-88ba-e053-2a91aa0a130245700112-2458-119a-e054-00144ff88e882018-12-26WarningsExact identifier
spl id: 7dec8140-064c-88ba-e053-2a91aa0a1302
spl set id: 45700112-2458-119a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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