FDA.reportPublic FDA data

Orbit Hand Sanitizer

Manufacturer
ORBIT CAPITAL LLC
Effective date
2020-08-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:44

Label at a glance#

ProductOrbit Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

▪ For hand-washing to decrease bacteria on the skin. ▪ Recommended for repeated use. ▪ Avoid contact with broken skin. ▪ Do not inhale or ingest.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6 years, use only under adult supervision. Not a recommendation for infants

Storage and handling

Do not store above 105°F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol (70%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerine, DM Sterile water, Carbomer, Vitamin E, Aloe Extract, H2O2, Triethanolamine

Uses

INDICATIONS & USAGE SECTION

▪ For hand-washing to decrease bacteria on the skin.

▪ Recommended for repeated use.

▪ Avoid contact with broken skin.

▪ Do not inhale or ingest.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105°F

May discolor some fabrics

Harmful to wood finishes and plastics

Questions?

OTC - QUESTIONS SECTION

+1(877)793-8998

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY - HANDS

Flammable. Keep away from heat and flame.

When using this product • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if skin irritates develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keeps out of reach of children. If swallowed, get medical help or contact a Poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6 years, use only under adult supervision.

Not a recommendation for infants

SPL UNCLASSIFIED SECTION

Instant HAND SANITIZER with MOISTURIZERS & VITAMIN E

KILLS ILLNESS CAUSING GERMS UPTO 99.9%

Manufactured and Distributed

by: Orbit Capital, LLC.Stafford, Texas.

www.orbitcapitalllc.com

Made in USA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014638isopropyl alcohol 70 % Topical SprayPSN1
1014638isopropyl alcohol 0.7 ML/ML Topical SpraySCD1
1014638isopropyl alcohol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78752-698-012023-01-30C16284748780-1f386c649-fbb0-0266-e053-dadaa90a7c1aORBIT HAND SANITIZER
78752-698-122023-01-30C16284748780-1f386c649-fbb0-0266-e053-dadaa90a7c1aORBIT HAND SANITIZER
78752-698-222023-01-30C16284748780-1f386c649-fbb0-0266-e053-dadaa90a7c1aORBIT HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78752-698-01Orbit Hand Sanitizer60 mL in 1 BOTTLE, SPRAYSPRAY601
78752-698-12Orbit Hand Sanitizer24 in 1 BOXSPRAY241
78752-698-22Orbit Hand Sanitizer6 in 1 CASESPRAY61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78752-698ORBIT HAND SANITIZER (ISOPROPYL ALCOHOL) SPRAY [ORBIT CAPITAL LLC]1Legacy NDC, 3 package rows20200908_f762f9c0-d910-4d28-9927-16b01ed284e7.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78752-69878752-698-01, 78752-698-12, 78752-698-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALOEV5VD430YW9IACT
HYDROGEN PEROXIDEBBX060AN9VIACT
TROLAMINE9O3K93S3TKIACT

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
c4000634-dfe5-43e5-baf6-2b4d201cbc01f762f9c0-d910-4d28-9927-16b01ed284e72020-08-27WarningsExact identifier
spl id: c4000634-dfe5-43e5-baf6-2b4d201cbc01
spl set id: f762f9c0-d910-4d28-9927-16b01ed284e7

Reported adverse events (FAERS/openFDA)#

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