FDA.reportPublic FDA data

BYD CARE Hand Sanitizer XD-A04

Manufacturer
Shanwei BYD Industrial Co Ltd
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:09

Label at a glance#

ProductBYD CARE Hand Sanitizer XD-A04
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

To Help decrease germs on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly without wiping until they are dry. For children under 6, use only under adult supervision. Not recommended for infants.

Storage and handling

After unseal, tighten the cap and use product within the validity period. After use, seal and keep away from light and moisture. Store in a cool and dry place. Do not store above 37 o C (98.6 o F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Distributed by Global Healthcare Product Solutions, LLC

1 (800) 293-2886

Manufactured by:

Shanwei BYD Industrial Co., Ltd.

Shanwei High-Tech Development Zone, Shanwei, China

Tel: +86-755-89888888

Website: www.byd.com 1313

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Alcohol 72% (V/V) 0101

Purpose:

OTC - PURPOSE SECTION

Antiseptic 0202

Uses:

INDICATIONS & USAGE SECTION

To Help decrease germs on the skin that could cause disease. Recommended for repeated use. 0303

Warnings:

WARNINGS SECTION

For external use only: hands

Flammable, Keep away from fire or flame. 0404

When using this product:

OTC - DO NOT USE SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
  • Do not inhale or ingest.
  • Use with caution if allergic. 0505

When using this product:

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
  • Do not inhale or ingest.
  • Use with caution if allergic. 0606

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • Irritation or redness develops.
  • Condition persists for more than 72 hours. 0707

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. 0808

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly without wiping until they are dry.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants. 0909

Other information:

STORAGE AND HANDLING SECTION

  • After unseal, tighten the cap and use product within the validity period.
  • After use, seal and keep away from light and moisture.
  • Store in a cool and dry place. Do not store above 37 oC (98.6 oF). 1010

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Arcylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethylpropanol, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Tocopheryl Acetate, Water 1111

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 mL NDC: 73818-100-01 1212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73818-100-012023-07-05C16284748780-1d6a99b39-bffe-a426-e053-dadaa90af4c2a5272e81-49a1-77e0-e053-2995a90aedb9
73818-100-012022-01-28C16284748780-1d6a99b39-bffe-a426-e053-dadaa90af4c2a5272e81-49a1-77e0-e053-2995a90aedb9

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73818-10073818-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
ISOPROPYL ALCOHOLND2M416302IACT

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
ffb6da56-b53b-dd9b-e053-6394a90a366ca5272e81-49a1-77e0-e053-2995a90aedb92023-07-05WarningsExact identifier
spl set id: a5272e81-49a1-77e0-e053-2995a90aedb9

Reported adverse events (FAERS/openFDA)#

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