FDA.reportPublic FDA data

TRUMED Hand Sanitizer

Manufacturer
GURUNANDA, LLC | GURUNANDA,LLC | Huzhou Yufan Cosmetics Technology Co., Ltd
Effective date
2021-06-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:40:48

Label at a glance#

ProductTRUMED Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredientActive ingredientEthyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

Flamable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact , rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appears.

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 rright away.

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly and rub together until dry. No towels needed.

OTHER SAFETY INFORMATION

Store below 110 F (43 C)

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Triethanolamine, 2-Dimethylaminoethanol, Aloe Barbadensis leaf Extract.

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Product image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product ImageProduct Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70708-009-012025-11-11C16284748780-1f386c64a-4083-0266-e053-dadaa90a7c1aHAND SANITIZER
70708-009-012023-01-30C16284748780-1f386c64a-4083-0266-e053-dadaa90a7c1aHAND SANITIZER

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70708-009TRUMED HAND SANITIZER (HAND SANITIZER) GEL [GURUNANDA, LLC]2Legacy NDC20210615_a64a539d-c5e2-59ec-e053-2a95a90a5e44.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
70708-00970708-009-01

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
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
ALOEV5VD430YW9IACT
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
567e4c4f-649a-c806-e063-6394a90a1bb7a64a539d-c5e2-59ec-e053-2a95a90a5e442026-07-13WarningsExact identifier
spl set id: a64a539d-c5e2-59ec-e053-2a95a90a5e44

Reported adverse events (FAERS/openFDA)#

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