FDA.reportPublic FDA data

hand sanitizer

Manufacturer
Ningbo dingchi Intelligent Manufacturing Technology Co., Ltd.
Effective date
2021-03-10
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 23:38:56

Label at a glance#

Producthand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106°F. (41°C) May discolor certain fabrics or surfaces

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

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.
For external use only.

When using this product, do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Stop use and ask doctor if irritation or rash appears and lasts.
Keep out of reach for children. If swallowed, get medical help or contact a

Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

do not use in or near the eyes.

When using this product

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store below 106°F. (41°C)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Lavandula Angustufolia(Lavender) Flower Extract, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine,D&C Red No.33,FD&C Blue No I, 2-(Dimethylamino) Ethanol.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75701-008-09 1800ml75701-008-09 1800ml75701-008-04 80ml75701-008-04 80ml75701-008-03 60ml75701-008-03 60ml75701-008-01 30ml75701-008-01 30ml75701-008-05 100ml75701-008-05 100ml75701-008-10 3780ml75701-008-10 3780ml75701-008-08 1000ml75701-008-08 1000ml75701-008-07 500ml75701-008-07 500ml75701-008-02 54ml75701-008-02 54ml75701-008-03 60ml75701-008-03 60ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN12
582753ethanol 0.7 ML/ML Topical SolutionSCD12
582753ethanol 70 % Topical SolutionSY12
582753ethyl alcohol 70 % Topical SolutionSY12

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75701-008-012022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-022022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-032022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-042022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-052022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-062022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-072022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-082022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-092022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer
75701-008-102022-07-29C16284748780-1e4f33bdf-a583-d8a0-e053-dadaa90a6e4e75701-008 hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75701-008-01hand sanitizer30 mL in 1 BOTTLELIQUID3012
75701-008-02hand sanitizer54 mL in 1 BOTTLELIQUID5412
75701-008-03hand sanitizer60 mL in 1 BOTTLELIQUID6012
75701-008-04hand sanitizer80 mL in 1 BOTTLELIQUID8012
75701-008-05hand sanitizer100 mL in 1 BOTTLELIQUID10012
75701-008-06hand sanitizer237 mL in 1 BOTTLELIQUID23712
75701-008-07hand sanitizer500 mL in 1 BOTTLELIQUID50012
75701-008-08hand sanitizer1000 mL in 1 BOTTLELIQUID100012
75701-008-09hand sanitizer1800 mL in 1 BOTTLELIQUID180012
75701-008-10hand sanitizer3780 mL in 1 BOTTLELIQUID378012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75701-008HAND SANITIZER LIQUID [NINGBO DINGCHI INTELLIGENT MANUFACTURING TECHNOLOGY CO., LTD.]12Legacy NDC, 10 package rows20210312_b0715bcf-a20c-bbbe-e053-2995a90a7a2c.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75701-00875701-008-05, 75701-008-10, 75701-008-01, 75701-008-07, 75701-008-06, 75701-008-08, 75701-008-09, 75701-008-02, 75701-008-03, 75701-008-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
D&C RED NO. 339DBA0SBB0LIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
DEANOL2N6K9DRA24IACT
LAVANDULA ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ALCOHOL3K9958V90MACTIB

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
bd3a59d9-ea1a-f4dc-e053-2a95a90a72cab0715bcf-a20c-bbbe-e053-2995a90a7a2c2021-03-10WarningsExact identifier
spl id: bd3a59d9-ea1a-f4dc-e053-2a95a90a72ca
spl set id: b0715bcf-a20c-bbbe-e053-2995a90a7a2c

Reported adverse events (FAERS/openFDA)#

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