Hand Sanitizer CHRISTMAS MEMORIES

Manufacturer
TAICORP ENTERPRISES LIMITED
Effective date
2020-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:51

Label at a glance#

ProductHand Sanitizer CHRISTMAS MEMORIES
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Dispense enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammability warning. Keep away from heat or flame.

Do not useon children less than 2 years of age (unless directed by a doctor).

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and consult a doctor if irritation develops.

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

  • Dispense enough product in your palm to thoroughly cover your hands.
  • Rub hands together briskly until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Extract, Cinnamon Essential Oil, Clove Essential Oil, Ginger Essential Oil, Glycerin, Sweet Orange Essential Oil, Vanilla Essential Oil, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014638isopropyl alcohol 70 % Topical SprayPSN1
1014638isopropyl alcohol 0.7 ML/ML Topical SpraySCD1
1014638isopropyl alcohol 70 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79883-010-01Hand Sanitizer CHRISTMAS MEMORIES60 mL in 1 BOTTLE, PLASTICSPRAY601
79883-010-02Hand Sanitizer CHRISTMAS MEMORIES120 mL in 1 BOTTLE, PLASTICSPRAY1201
79883-010-03Hand Sanitizer CHRISTMAS MEMORIES250 mL in 1 BOTTLE, PLASTICSPRAY2501
79883-010-04Hand Sanitizer CHRISTMAS MEMORIES500 mL in 1 BOTTLE, PLASTICSPRAY5001
79883-010-05Hand Sanitizer CHRISTMAS MEMORIES1000 mL in 1 BOTTLE, PLASTICSPRAY10001
79883-010-06Hand Sanitizer CHRISTMAS MEMORIES120 mL in 1 BOTTLE, PLASTICSPRAY1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79883-010HAND SANITIZER CHRISTMAS MEMORIES (ISOPROPYL ALCOHOL) SPRAY [TAICORP ENTERPRISES LIMITED]1Legacy NDC, 6 package rows20201003_3e5373ba-1afc-457a-a9dd-25ef142ca3f5.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79883-01079883-010-01, 79883-010-02, 79883-010-03, 79883-010-04, 79883-010-05, 79883-010-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
fe117ce0-9e26-4f7e-96d0-a46b15d6e8943e5373ba-1afc-457a-a9dd-25ef142ca3f52020-08-25WarningsExact identifier
spl id: fe117ce0-9e26-4f7e-96d0-a46b15d6e894
spl set id: 3e5373ba-1afc-457a-a9dd-25ef142ca3f5

Reported adverse events (FAERS/openFDA)#

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