FDA.reportPublic FDA data

HER LH2476 Citrus Scented Hand Sanitizer Kit

Manufacturer
HER ACCESSORIES
Effective date
2023-10-26
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:23:08

Label at a glance#

ProductHER LH2476 Citrus Scented Hand Sanitizer Kit
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Place a 'palmful' of product in one hand Spread on both hands and rub the skin until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 68%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on hands.

Warnings

WARNINGS SECTION

​For external use only

Flammable, keep away from fire or flame

irritation and redness develops. Stop use and ask a doctor if

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place a 'palmful' of product in one hand
  • Spread on both hands and rub the skin until dry

Other Information

OTHER SAFETY INFORMATION

To report a serious adverse reaction please write to HER Accessories 10 West 33rd. St. New York, NY 10001

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, carbomer, sodium hydroxide, may contain: red 33, blue 1, yellow 5.

HER LH2476 Citrus Scented Hand Sanitizer Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AngelAngel

DevilDevil

PackagingPackaging

Packaging2Packaging2

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
70589-10470589-104-01
70589-10570589-105-01

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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
0fc64685-771f-d21c-e063-6394a90aea753338cede-2112-4540-a8af-e435db9df3a22024-01-25WarningsExact identifier
spl set id: 3338cede-2112-4540-a8af-e435db9df3a2

Reported adverse events (FAERS/openFDA)#

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