HAND SANITIZER

Manufacturer
TRI-COASTAL DESIGN GROUP INC.
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:39

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure14 sections

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

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 open flame and sources of heat

■ Does not contain grain alcohol; do not drink. If taken internally will produce gastric distrubances.

When using this product

OTC - WHEN USING SECTION

■ Avoid the eyes and mucoous membranes

■ In the case of eyes or mucous membranes contacr, rinse area thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ Condition worsens

■ Redness or irritation develops

■ Condition persists for more than 3 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ If swallowed, contact a doctor or Poison Control Center immediately

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

SPL UNCLASSIFIED SECTION

■ Store below 105ºF

■ May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance, PEG-40 Hydrogenated Castor Oil, FD&C YELLOW NO.5, D&C RED N0.33

Questions?

OTC - QUESTIONS SECTION

■ 1-800-278-9218

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49852-702-012022-01-28C16284748780-1d6a99b39-c648-a426-e053-dadaa90af4c2TricstlFrtressIvryOrngYllwlHndSntzrAlch62

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49852-702-01HAND SANITIZER30 mL in 1 BOTTLEGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49852-702HAND SANITIZER GEL [TRI-COASTAL DESIGN GROUP INC.]2Legacy NDC, 1 package rows20200804_abfb4e39-a96d-b1a9-e053-2a95a90ab16a.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49852-70249852-702-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
abfe13b7-ac6b-b919-e053-2995a90aa8b5abfb4e39-a96d-b1a9-e053-2a95a90ab16a2020-08-03WarningsExact identifier
spl id: abfe13b7-ac6b-b919-e053-2995a90aa8b5
spl set id: abfb4e39-a96d-b1a9-e053-2a95a90ab16a

Reported adverse events (FAERS/openFDA)#

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