PURE PERFECT SANITIZER

Manufacturer
Buddy Co., Ltd.
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:59

Label at a glance#

ProductPURE PERFECT SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Uses: Disinfection of hands and skin

Dosage and administration

Directions: Spray an appropriate amount on your hands and rub thoroughly to dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ALCOHOL 70.0 w%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Water, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Sodium Hyaluronate, Camellia Sinesis Leaf Extract, Morus Alba Bark Extract, Aloe Barbadensis, Leaf Extract, Olea Europaea(Olive) Fruit Oil, Tocopheryl Acetate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Antiseptic

WARNINGS

WARNINGS SECTION

Warnings:

1. Do not use the product on the following areas :
Around the eyes and ears, in the mouth, large body part and damaged skin(it may cause irritation.)
2. If you suffer from the next symptom, discontinue use of the product immediately and consult a physician or pharmacist.
1) Hypersensitivity symptoms e.g. rash, erythema, itchiness, and edema
2) Skin irritation symptoms

3. Other precautions
1) For external use only. (Do not swllow.)
2) Avoid contact with eyes. If it contacts with eyes, wash with clean clean water and consult a physician or a pharmacist.
3) Be careful not to inhale vapors in case of using for a long time.
(In case of inhaling large amounts of ethanol vapor, it may cause irritation of the mucous membranes and headaches.)
(Limited to ethanol-containing the product)
4) If you use this product on the same area repeatedly, cure should be provided as the skin may become rough due to excessive oil removal.
5) Do not use sealed bandages, cast bandages, or packs as they many cause irritation.
6) Do not use this drug on the anal or vagina areas, or with hot packs, as it may cause irritation or chemical burns.
7) Use only for the intended purpose.

4. Precaution for storage
1) Keep away from direct sunlight and do not expose the product to heating devices or flame.
2) Let the children not touch this drug and in case of swallowing it, go to the hospital immediately.
3) After use. close the lid completely and prevent the product from drying or foreign objects from getting inside the container.
4) In case of keeping the product on the different container, it may cause accidents or deterioration of quality.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

Uses:
Disinfection of hands and skin

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

Spray an appropriate amount on your hands and rub thoroughly to dry.

Other information

OTHER SAFETY INFORMATION

Other information
■ Read directions and precautions before use.
■ Avoid freezing and excessive heat above 40℃.

PACKAGE LABEL - PURE PERFECT SANITIZER GEL 50mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

PACKAGE LABEL - PURE PERFECT SANITIZER GEL 500mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809476030465GTIN-13: 8809476030465
EAN-13: 8809476030465
GTIN storage (14 digits): 08809476030465
500 bottle.jpg
BarcodeEAN-138809476030496GTIN-13: 8809476030496
EAN-13: 8809476030496
GTIN storage (14 digits): 08809476030496
50 container.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74716-010-012022-01-28C16284748780-1d6a99b39-bd45-a426-e053-dadaa90af4c2027a044b-3275-43bd-9a18-38bf636a0e0f
74716-010-022022-01-28C16284748780-1d6a99b39-bd45-a426-e053-dadaa90af4c2027a044b-3275-43bd-9a18-38bf636a0e0f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74716-010-01PURE PERFECT SANITIZER50 mL in 1 CONTAINERGEL501
74716-010-02PURE PERFECT SANITIZER500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74716-010PURE PERFECT SANITIZER (ALCOHOL) GEL [BUDDY CO., LTD.]1Legacy NDC, 2 package rows20200413_027a044b-3275-43bd-9a18-38bf636a0e0f.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74716-01074716-010-01, 74716-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
77d64b26-554d-4658-b837-298d03df5e5e027a044b-3275-43bd-9a18-38bf636a0e0f2020-04-13WarningsExact identifier
spl id: 77d64b26-554d-4658-b837-298d03df5e5e
spl set id: 027a044b-3275-43bd-9a18-38bf636a0e0f

Reported adverse events (FAERS/openFDA)#

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