FDA.reportPublic FDA data

Apollo Instant Hand Sanitizer

Manufacturer
Sbu Group L.P. DBA Apollo Distributors | NINGBO UNICE HOUSEWARES CO. LTD | AOGRAND INTERNATIONAL TRADE CORPORATION | Guangzhou Orchard Aromatherapy & Skin Care Co Ltd | Guangzhou Xuelei Cosmetic Co., Ltd
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:21:27

Label at a glance#

ProductApollo Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help decrease bactrerial 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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help decrease bactrerial 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.

When using this product,

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

SPL UNCLASSIFIED SECTION

  • Store below 110 °F (43 °C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Triethanolamine, Glycerin, Water.

Package Labeling :500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Package Labeling :237ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling :60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling :120ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling :5000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78303-000-022022-01-28C16284748780-1d6a99b39-c489-a426-e053-dadaa90af4c2Apollo Instant Hand Sanitizer
78303-000-042022-01-28C16284748780-1d6a99b39-c489-a426-e053-dadaa90af4c2Apollo Instant Hand Sanitizer
78303-000-082022-01-28C16284748780-1d6a99b39-c489-a426-e053-dadaa90af4c2Apollo Instant Hand Sanitizer
78303-000-132022-01-28C16284748780-1d6a99b39-c489-a426-e053-dadaa90af4c2Apollo Instant Hand Sanitizer
78303-000-162022-01-28C16284748780-1d6a99b39-c489-a426-e053-dadaa90af4c2Apollo Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78303-000-02Apollo Instant Hand Sanitizer60 mL in 1 BOTTLEGEL602
78303-000-04Apollo Instant Hand Sanitizer120 mL in 1 BOTTLEGEL1202
78303-000-08Apollo Instant Hand Sanitizer237 mL in 1 BOTTLEGEL2372
78303-000-13Apollo Instant Hand Sanitizer5000 mL in 1 BOTTLEGEL50002
78303-000-16Apollo Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78303-000APOLLO INSTANT HAND SANITIZER (ALCOHOL) GEL [SBU GROUP L.P. DBA APOLLO DISTRIBUTORS]2Legacy NDC, 5 package rows20200715_b4100cc4-1458-4a9c-8bb5-a5ad5d3372a3.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78303-00078303-000-16, 78303-000-08, 78303-000-02, 78303-000-04, 78303-000-13

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
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
aa684bea-80d2-e56c-e053-2995a90a24a4b4100cc4-1458-4a9c-8bb5-a5ad5d3372a32020-07-14WarningsExact identifier
spl id: aa684bea-80d2-e56c-e053-2995a90a24a4
spl set id: b4100cc4-1458-4a9c-8bb5-a5ad5d3372a3

Reported adverse events (FAERS/openFDA)#

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