FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
SINGWONG ASIA PACIFIC (BOLUO) CO., LTD.
Effective date
2020-09-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:16:16

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

put enough product in your palm to cover hands and rub hands together briskly until dry. children under 6 years of age should be supervised.

Storage and handling

Store below 86F/30C May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 76% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame

For external use only

WARNINGS SECTION

For external use only

stop use and ask a doctor if

OTC - DO NOT USE SECTION

irritation or rash appears and lasts

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.

OTC - STOP USE SECTION

Stop use and ask a 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 of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

put enough product in your palm to cover hands and rub hands together briskly until dry.

children under 6 years of age should be supervised.

Other information

STORAGE AND HANDLING SECTION

  • Store below 86F/30C
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water,glycerin,sodium polyacylate(2500000MW),aloe

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75283-006-0175283-006-0175283-006-0275283-006-0275283-006-0375283-006-0375283-006-0475283-006-0475283-006-0575283-006-0575283-006-0675283-006-0675283-006-0775283-006-0775283-006-0875283-006-08

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75283-00675283-006-01, 75283-006-02, 75283-006-03, 75283-006-04, 75283-006-05, 75283-006-06, 75283-006-07, 75283-006-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
GLYCERINPDC6A3C0OXIACT
ALOEV5VD430YW9IACT
WATER059QF0KO0RIACT
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
b8d6989c-f62a-28a7-e053-2995a90ad682a374a634-0bbe-0abb-e053-2995a90aaed42021-01-14WarningsExact identifier
spl set id: a374a634-0bbe-0abb-e053-2995a90aaed4

Reported adverse events (FAERS/openFDA)#

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