Hand Sanitizer Wipes

Manufacturer
Shenzhen Lantern Scicence Co.,Ltd. | Shenzhen Lantern Science Co.,Ltd.
Effective date
2025-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:10:21

Label at a glance#

ProductHand Sanitizer Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizing to decrease bacteria on skin. Recommended for repeated use.

Dosage and administration

Tear open package and unfold wipe. Thoroughly wipe hands, fingers and wrists. Be sure to use entire wipe for approximately 20 seconds. No rinsing or toweling is required. Discard after single use. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

lsopropyl Alcohol 70%.........Antiseptic

Uses

OTC - PURPOSE SECTION

Hand sanitizing to decrease bacteria on skin.
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only.
Flammable, keep away from fire or flame.
Do not use this product in or near eyes. lf contact occursrinse thoroughly with water.

Keep out of reach of children unless under adult supervision.

Discontinue use if skin irritation and redness develop.

If condition persists for more than 72 hoursconsult a physician.

Directions

INDICATIONS & USAGE SECTION

Tear open package and unfold wipe.
Thoroughly wipe hands, fingers and wrists.
Be sure to use entire wipe for approximately 20 seconds.

No rinsing or toweling is required.

Discard after single use. Do not flush.

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision..Discontinue use if skin irritation and redness develop.

other Information

OTHER SAFETY INFORMATION

Store below 104°F(40°)
May discolor some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), Glycerine.Hydrogen Peroxide.

packing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packingPackagingPackaging

packing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packingpackingpacking

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-494-01Hand Sanitizer Wipes30 in 1 BOXCLOTH301
54860-494-02Hand Sanitizer Wipes100 in 1 BOXCLOTH1001

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-49454860-494-01, 54860-494-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
Hand Sanitizer WipesISOPROPYL ALCOHOLShenzhen Lantern Scicence Co.,Ltd.3c37f72b-623c-c8f6-e063-6294a90a971e2025-08-12WarningsExact identifier
ndc (package): 54860-494-02
ndc (package): 54860-494-01
ndc (product): 54860-494
ndc11 (package): 54860049402
ndc11 (package): 54860049401
spl id: 3c37c465-5008-8a82-e063-6294a90a32a2
spl set id: 3c37f72b-623c-c8f6-e063-6294a90a971e

Reported adverse events (FAERS/openFDA)#

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