Hand Sanitizer with Clip

Manufacturer
China Ningbo Shangge Technology Co., Ltd.
Effective date
2020-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:27

Label at a glance#

ProductHand Sanitizer with Clip 1.8oz
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hand thoroughly with product briskly rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store at room temperature may discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from heat and flame

Do not use

OTC - DO NOT USE SECTION

  • in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rednees develp and persist 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hand thoroughly with product
  • briskly rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature
  • may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate.

OTC - QUESTIONS SECTION

1-855-345-5575

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel 2label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58503-151-012024-01-30C16284748780-11030e365-4bbd-111a-e063-dadaa90a10e2b06b1dcf-f034-5978-e053-2995a90a41fe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58503-151-01Hand Sanitizer with Clip1.8oz1 in 1 PACKAGELIQUID11
58503-151-01Hand Sanitizer with Clip1.8oz53 mL in 1 BOTTLELIQUID531

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58503-151HAND SANITIZER WITH CLIP 1.8OZ (ALCOHOL) LIQUID [CHINA NINGBO SHANGGE TECHNOLOGY CO., LTD.]1Legacy NDC, 2 package rows20200929_b06b1dcf-f034-5978-e053-2995a90a41fe.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
58503-15158503-151-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
b06b1dcf-f033-5978-e053-2995a90a41feb06b1dcf-f034-5978-e053-2995a90a41fe2020-09-28WarningsExact identifier
spl id: b06b1dcf-f033-5978-e053-2995a90a41fe
spl set id: b06b1dcf-f034-5978-e053-2995a90a41fe

Reported adverse events (FAERS/openFDA)#

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