FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
GUANGZHOU CANYON BIOTECHNOLOGY CO.,LTD
Effective date
2022-01-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:10:53

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

Srore below 105F May discolor some fabric

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For Hand Sanitizer to decrease bacteria on the skin

Recommended for repeat use

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flame

Does not contain grain clcohol, do not drink, If taken internally wil product serious gastric disturbances.

Do not use

OTC - DO NOT USE SECTION

  • Does not contain grain clcohol, do not drink, If taken internally wil product serious gastric disturbances.

When using this product

OTC - WHEN USING SECTION

When using this product

Avoid the eyes and mucousmembranes.

In the case of eyes or mucous membranes contact, rinse area thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

Redness or irriation develops

Condtitions worsens

If condition persists for more than 3 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed conteact 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 products

-In the case of eye contact, rinse eyes thoroughly with water.

Other information

STORAGE AND HANDLING SECTION

  • Srore below 105F
  • May discolor some fabric

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance , Carbomer, Aloe Extract, Sodium Hydroxide, Yellow 5

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75675-009-01 30ml75675-009-01 30ml75675-009-02 45ml75675-009-02 45ml75675-009-03 60ml75675-009-03 60ml75675-009-04 90ml75675-009-04 90ml75675-009-05 120ml75675-009-05 120ml75675-009-06 225ml75675-009-06 225ml75675-009-07 240ml75675-009-07 240ml75675-009-08 250ml75675-009-08 250ml75675-009-09 360ml75675-009-09 360ml75675-009-10 500ml75675-009-10 500ml75675-009-11 1000ml75675-009-11 1000ml75675-009-12 1500ml75675-009-12 1500ml75675-009-13 1800ml75675-009-13 1800ml75675-009-14 3780ml75675-009-14 3780ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75675-009-012022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-022022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-032022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-042022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-052022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-062022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-072022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-082022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-092022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-102022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-112022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-122022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-132022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-142022-01-30C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-012022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-022022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-032022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-042022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-052022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-062022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-072022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-082022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-092022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-102022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-112022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-122022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-132022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009
75675-009-142022-01-28C16284748780-1d6a99b39-c988-a426-e053-dadaa90af4c275675-009

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
75675-00975675-009-04, 75675-009-05, 75675-009-06, 75675-009-07, 75675-009-08, 75675-009-09, 75675-009-10, 75675-009-14, 75675-009-01, 75675-009-11, 75675-009-02, 75675-009-03, 75675-009-12, 75675-009-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C BLUE NO. 1H3R47K3TBDIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOEV5VD430YW9IACT
SODIUM HYDROXIDE55X04QC32IIACT

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
e2bb1495-3ad8-3a9c-e053-2a95a90a3740b0ab4e89-9d96-d9fa-e053-2995a90a2afa2022-07-01WarningsExact identifier
spl set id: b0ab4e89-9d96-d9fa-e053-2995a90a2afa

Reported adverse events (FAERS/openFDA)#

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