FDA.reportPublic FDA data

apollo Instant Hand Sanitizer

Manufacturer
Sbu Group L.P. | GUANGZHOU XUELEI COSMETIC CO.,LTD.
Effective date
2021-11-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:44:50

Label at a glance#

Productapollo Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help decrease bacterial on the skin, when water, soap& towel are not available. Recommended for repeated use.

Dosage and administration

Place enough product into your palms and thoroughly spread on both hands. Rub into skin until dry.

Storage and handling

Store below 110℉（43℃） May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacterial on the skin, when water, soap& towel are not available.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

OTC - WHEN USING SECTION

When using this product,

Avoid contact with eyes. In case of contact flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor

If redness or irritation develop and persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product into your palms and thoroughly spread on both hands.

Rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

Store below 110℉（43℃）

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Triethanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

apollo

Instant Hand Sanitizer

Anti Bacterial

Contains 75 % Alcohol

2 FL OZ (60ml)

Kills 99% Germs

NDC: 78303-001-01

60ML Label60ML Label

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

apollo

Instant Hand Sanitizer

Anti Bacterial

Contains 75 % Alcohol

1.29 Gallons

5,000 ML

Kills 99% Germs

NDC: 78303-001-02

5000ML Label5000ML Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN4
1305100ethanol 0.75 ML/ML Topical GelSCD4
1305100ethanol 75 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78303-001-012023-01-30C16284748780-1f386c649-dde7-0266-e053-dadaa90a7c1aapollo Instant Hand Sanitizer
78303-001-022023-01-30C16284748780-1f386c649-dde7-0266-e053-dadaa90a7c1aapollo Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78303-001-01apollo Instant Hand Sanitizer60 mL in 1 BOTTLEGEL604
78303-001-02apollo Instant Hand Sanitizer5000 mL in 1 BOTTLEGEL50004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78303-001APOLLO INSTANT HAND SANITIZER (INSTANT HAND SANITIZER) GEL [SBU GROUP L.P.]4Legacy NDC, 2 package rows20211110_a6976e49-aa6d-0aaf-e053-2a95a90aa065.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78303-00178303-001-01, 78303-001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
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
d0524f5c-09e4-c7ff-e053-2a95a90a04dea6976e49-aa6d-0aaf-e053-2a95a90aa0652021-11-08WarningsExact identifier
spl id: d0524f5c-09e4-c7ff-e053-2a95a90a04de
spl set id: a6976e49-aa6d-0aaf-e053-2a95a90aa065

Reported adverse events (FAERS/openFDA)#

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