FDA.reportPublic FDA data

TRUMED Instant Hand Sanitizer

Manufacturer
GURUNANDA LLC
Effective date
2022-08-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:50:35

Label at a glance#

ProductTRUMED Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

PRODUCT LABELPRODUCT LABEL

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

FOR EXTERNAL USE ONLY

Flammable. Keep away from heat or flame.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes,ears, mouth or open skin wounds. In case of contact, rinse the area thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts for more than 72 hours.

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. Poison Control can be reached at (800) 222-1222

DOSAGE & ADMINISTRATION SECTION

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

-No towel needed.

-Supervise children under 6 years when using this product to avoid swallowing.

OTHER SAFETY INFORMATION

Store below 110° F (43° C)

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aminomethyl Propanol , Fragrance, 2-Dimethylaminoethanol

INDICATIONS & USAGE SECTION

Helps to reduce bacteria on skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRODUCT DISPLAYPRODUCT DISPLAY

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70708-800-012025-11-10C16284748780-10191ceaa-62b6-198a-e063-dbdaa90aec3eTruMed Instant Hand Sanitizer
70708-800-012023-07-28C16284748780-10191ceaa-62b6-198a-e063-dbdaa90aec3eTruMed Instant Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70708-800TRUMED INSTANT HAND SANITIZER (HAND SANITIZER) GEL [GURUNANDA LLC]3Legacy NDC20220902_b68f101d-1704-edfe-e053-2a95a90a13c5.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
70708-80070708-800-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT
LAVENDER OILZBP1YXW0H8IACT
CARBOMER 9404Q93RCW27EIACT
DEANOL2N6K9DRA24IACT

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
4348b518-e634-048b-e063-6294a90a8b58b68f101d-1704-edfe-e053-2a95a90a13c52025-11-10WarningsExact identifier
spl set id: b68f101d-1704-edfe-e053-2a95a90a13c5

Reported adverse events (FAERS/openFDA)#

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