FDA.reportPublic FDA data

BioTide Antiseptic Hand Sanitizer Gel

Manufacturer
Bioriginal Food & Science Corp
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:09:12

Label at a glance#

ProductBioTide Antiseptic Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire or flame.

Do not use 

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 59-86°F (15-30°C)
  • avoid freezing and excessive heat above 104°F (40°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, glycerin, carbomer 940, d-alpha tocopherol acetate, fragrance, glitter (rayon, glycerin, water, urea, shellac, mica, titanium dioxide, ferric ammonium ferrocyanide, tin oxide), triethanolamine.

Questions or Comments?

OTC - QUESTIONS SECTION

949-622-9030

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

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
76815-00276815-002-04

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
REGENERATED CELLULOSEBX81F82EWGIACT
UREA8W8T17847WIACT
SHELLAC46N107B71OIACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FERRIC AMMONIUM FERROCYANIDE9R0NVI936IIACT
STANNIC OXIDEKM7N50LOS6IACT
TROLAMINE9O3K93S3TKIACT
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
cf35bf38-069e-174c-e053-2995a90acf80b25cc7df-9b97-35fa-e053-2a95a90a17952021-10-25WarningsExact identifier
spl set id: b25cc7df-9b97-35fa-e053-2a95a90a1795

Reported adverse events (FAERS/openFDA)#

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