Apollo Medical Products Disinfecting Wipes

Manufacturer
KKJ & Associates LLC
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:44

Label at a glance#

ProductApollo Medical Products Disinfecting Wipes
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Clean the affected area by using wipe to apply and clean skin or surface. Let air dry.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For first aid and for cleansing areas to reduce bacteria and viruses.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. Store at room temperature 59F-86F (15C-30C)

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. POISON CONTROL (800)-222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area by using wipe to apply and clean skin or surface. Let air dry.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water.

STORAGE AND HANDLING SECTION

Dispose of wipe in trash after use. Do not flush. Tightly close lids between uses to retain moisture. Nonrefillable container. Do not reuse or refill this empty container. Offer empty containers for recycling. If recycling is not available, discard container in trash.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79642-003-012022-01-28C16284748780-1d6a99b39-fb4f-a426-e053-dadaa90af4c2Apollo Disinfecting Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79642-003-01Apollo Medical Products Disinfecting Wipes1 in 1 CONTAINERLIQUID11
79642-003-01Apollo Medical Products Disinfecting Wipes500 mL in 1 CONTAINERLIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79642-003APOLLO MEDICAL PRODUCTS DISINFECTING WIPES (ALCOHOL) LIQUID [KKJ & ASSOCIATES LLC]1Legacy NDC, 2 package rows20200919_af84721f-0ee5-8f76-e053-2995a90a9f0f.zip

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
79642-00379642-003-01

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
af84721f-0ee4-8f76-e053-2995a90a9f0faf84721f-0ee5-8f76-e053-2995a90a9f0f2020-09-17WarningsExact identifier
spl id: af84721f-0ee4-8f76-e053-2995a90a9f0f
spl set id: af84721f-0ee5-8f76-e053-2995a90a9f0f

Reported adverse events (FAERS/openFDA)#

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