FDA.reportPublic FDA data

Senegence Hand Sanitizer

Manufacturer
SGII, Inc | 220 Laboratories inc
Effective date
2021-03-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:39:05

Label at a glance#

ProductSenegence Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Alcohol 70% v/v.........................Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Warnings

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do not use
• 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

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surfaces. Rub hands together until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.

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

Aqua/Water/Eau, Propanediol, Glycerin, Hydroxypropyl Guar, Nangai (Canarium Indicum) Seed Oil, Aloe Vera (Aloe Barbadensis) Leaf Juice, Kelp (Laminaria Digitata) Extract, Yeast (Saccharomyces Cerevisiae) Extract, Orchid (Orchis Mascula) Flower Extract, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer-2, Hydrolyzed Sodium Hyaluronate, Sodium Acetylated Hyaluronate, Tocopheryl Acetate, Panthenol, Glucosamine HCl, Retinyl Palmitate, Citric Acid, Denatonium Benzoate, T-Butyl Alcohol, Sodium Hydroxide, Alcohol Denat., Butylene Glycol, Urea*, Pentylene Glycol, Phenoxyethanol, Ethylhexylglycerin, Parfum/Fragrance, Hydroxycitronellal, Benzyl Salicylate, Limonene, Geraniol, Linalool, Isoeugenol. *Synthetic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72644-637-012024-07-30C16284748780-11030e365-197a-111a-e063-dadaa90a10e2Senegence Hand Sanitizer
72644-637-012024-01-30C16284748780-11030e365-197a-111a-e063-dadaa90a10e2Senegence Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72644-637-01Senegence Hand Sanitizer118 mL in 1 BOTTLELIQUID1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72644-637SENEGENCE HAND SANITIZER (ALCOHOL 70%) LIQUID [SGII, INC]2Legacy NDC, 1 package rows20210320_b0f0eecf-0182-82b6-e053-2a95a90ab936.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72644-63772644-637-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
LIMONENE, (+)-GFD7C86Q1WIACT
SODIUM HYDROXIDE55X04QC32IIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
UREA8W8T17847WIACT
PHENOXYETHANOLHIE492ZZ3TIACT
HYALURONATE SODIUMYSE9PPT4THIACT
CANARIUM INDICUM SEED OIL4UI31S9F33IACT
ALOE VERA LEAFZY81Z83H0XIACT
LAMINARIA DIGITATA15E7C67EE8IACT
ISOEUGENOL5M0MWY797UIACT
YEAST3NY3SM6B8UIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
PENTYLENE GLYCOL50C1307PZGIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
GERANIOLL837108USYIACT
LINALOOL, (+/-)-D81QY6I88EIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
PANTHENOLWV9CM0O67ZIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GUARAPROLOSE (1300 MPA.S AT 1%)1530WMS90SIACT
GLUCOSAMINE HYDROCHLORIDE750W5330FYIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ORCHIS MASCULA FLOWER6H1JQK35LAIACT

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
bde71227-297c-36f0-e053-2995a90ab9eeb0f0eecf-0182-82b6-e053-2a95a90ab9362021-03-19WarningsExact identifier
spl id: bde71227-297c-36f0-e053-2995a90ab9ee
spl set id: b0f0eecf-0182-82b6-e053-2a95a90ab936

Reported adverse events (FAERS/openFDA)#

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