Hand Sanitizer

Manufacturer
Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date
2023-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:57:37

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Rub dime sized amount between hands until dry. Supervise children in the use of this product. In the case of eye contact, rinse eyes thoroughly with water.

Storage and handling

Store below 106ºF (41 ºC). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

  • , keep away from fire and flame. Flammable
  • Does not contain grain alcohol; do not drink, if taken internally serious gastric disturbances will result.

When using this product

OTC - WHEN USING SECTION

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membranes contact, rinse area thoroughly with water
  • In case of deep or puncture wounds or serious burns, consult physician.
  • If redness, irritation, swelling or pain persists or increases or if infection occurs discontinue use and consult physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, contact a doctor or Poison Control Center immediately.

OTC - STOP USE SECTION

In case of irritation, discontinue use and consult your doctor.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Rub dime sized amount between hands until dry.
  • Supervise children in the use of this product.
  • In the case of eye contact, rinse eyes thoroughly with water.

Other Information:

STORAGE AND HANDLING SECTION

Store below 106ºF (41 ºC). May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl Propanol, Carbomer, Water.

​Questions?

OTC - QUESTIONS SECTION

  • 1-800-369-4670

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61805-110-01Hand Sanitizer50 mL in 1 BOTTLEGEL503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61805-110HAND SANITIZER (ALCOHOL) GEL [BATH CONCEPT COSMETICS (DONGGUAN) CO., LTD]3Current NDC, Legacy NDC, 1 package rows20231026_065e083f-3c13-495d-8619-df45c5fce68b.zip

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
61805-11061805-110-01

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 SanitizerALCOHOLBath Concept Cosmetics (Dongguan) Co., Ltd065e083f-3c13-495d-8619-df45c5fce68b2023-10-25WarningsExact identifier
ndc (package): 61805-110-01
ndc (product): 61805-110
ndc11 (package): 61805011001
spl id: 089656e4-6de0-7be7-e063-6394a90a7703
spl set id: 065e083f-3c13-495d-8619-df45c5fce68b

Reported adverse events (FAERS/openFDA)#

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