HER LH2475 Vanilla Scented Hand Sanitizer Kit

Manufacturer: HER ACCESSORIES
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: legacy-cache
Hydrated at: 2026-08-01 21:23:08

Label at a glance#

ProductHER LH2475 Vanilla 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 LH2475 Vanilla Scented Hand Sanitizer Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Products#

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

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

HER LH2475 Vanilla Scented Hand Sanitizer Kit
Alcohol
HER LH2475 Vanilla Scented Hand Sanitizer
SODIUM HYDROXIDE
D&C RED NO. 33
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70589-102	70589-102-01
70589-103	70589-103-01

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
Name	UNII	Kind
SODIUM HYDROXIDE	55X04QC32I	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0fc64685-771e-d21c-e063-6394a90aea75			1c68ac53-1049-46e5-a89e-5de2cc9aab43	2024-01-25	Warnings	Exact identifier spl set id: 1c68ac53-1049-46e5-a89e-5de2cc9aab43

Reported adverse events (FAERS/openFDA)#

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