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
3
Source
full-release
Hydrated at
2026-05-31 23:44:50

Label at a glance#

Productapollo Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 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%

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, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, Propylene Glycol, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Power, Lactic Acid, Citric Acid.

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785ml NDC: 74658-009-01

3785ML Label3785ML Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN3
1305100ethanol 0.75 ML/ML Topical GelSCD3
1305100ethanol 75 % Topical GelSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78303-002-012023-01-30C16284748780-1f386c64a-0c12-0266-e053-dadaa90a7c1aapollo Instant Hand Sanitizer (New Formulation)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78303-002-01apollo Instant Hand Sanitizer3785 mL in 1 BOTTLEGEL37853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78303-002APOLLO INSTANT HAND SANITIZER (INSTANT HAND SANITIZER) GEL [SBU GROUP L.P.]3Legacy NDC, 1 package rows20211110_a91a1b64-2993-4628-e053-2a95a90a86e6.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78303-00278303-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
LINALOOL, (+/-)-D81QY6I88EIACT
3-HEXENYL ACETATE, (3Z)-6INA6GC5I6IACT
3-HEXEN-1-OL, (3Z)-V14F8G75P4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
NEROL38G5P53250IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
TOCOPHEROLR0ZB2556P8IACT
GLYCERINPDC6A3C0OXIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
CYCLAMEN ALDEHYDE4U37UX0E1EIACT
LACTIC ACID33X04XA5ATIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
METHYL DIHYDROJASMONATE (SYNTHETIC)3GW44CIE3YIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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
d053875d-c1fd-17ea-e053-2995a90af95da91a1b64-2993-4628-e053-2a95a90a86e62021-11-08WarningsExact identifier
spl id: d053875d-c1fd-17ea-e053-2995a90af95d
spl set id: a91a1b64-2993-4628-e053-2a95a90a86e6

Reported adverse events (FAERS/openFDA)#

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