PopCare

Manufacturer
Ningbo The One Bio-technology Co., Ltd
Effective date
2021-01-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:32

Label at a glance#

ProductPopCare
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Lift tab at front of the lid to open. Pull up corner of center sheet and thread through dispenser slit in the lid. Pull up exposed wipe and snap off. The next wipe is ready for dispensing. Close lid to retaining moisture. T ake wipe and rub thoroughly over all surfaces of both hands. Rub hands briskly together to dry. Dispose of used wipe in trash. Do not Flush. Not recommended for infants

Storage and handling

Do not store above 105F/40C May discolor some fabrics Harmful to wooden finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - WHEN USING SECTION

When using the product

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor

if irritation or redness develops condition persists for more than 72 hours.

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

Lift tab at front of the lid to open.

Pull up corner of center sheet and thread through dispenser slit in the lid.

Pull up exposed wipe and snap off.

The next wipe is ready for dispensing.

Close lid to retaining moisture. T

ake wipe and rub thoroughly over all surfaces of both hands. Rub hands briskly together to dry.

Dispose of used wipe in trash.

Do not Flush.

Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F/40C

May discolor some fabrics

Harmful to wooden finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

R0 puter water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81478-001-012022-07-29C16284748780-1e4f33bdf-a410-d8a0-e053-dadaa90a6e4ePopCare
81478-001-022022-07-29C16284748780-1e4f33bdf-a410-d8a0-e053-dadaa90a6e4ePopCare
81478-001-032022-07-29C16284748780-1e4f33bdf-a410-d8a0-e053-dadaa90a6e4ePopCare
81478-001-042022-07-29C16284748780-1e4f33bdf-a410-d8a0-e053-dadaa90a6e4ePopCare
81478-001-052022-07-29C16284748780-1e4f33bdf-a410-d8a0-e053-dadaa90a6e4ePopCare

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81478-001-01PopCare2 mL in 1 CONTAINERCLOTH21
81478-001-01PopCare100 in 1 CONTAINERCLOTH1001
81478-001-02PopCare200 in 1 CONTAINERCLOTH2001
81478-001-02PopCare2 mL in 1 CONTAINERCLOTH21
81478-001-03PopCare80 in 1 BOTTLECLOTH801
81478-001-03PopCare160 mL in 1 CONTAINERCLOTH1601
81478-001-04PopCare200 mL in 1 BOTTLECLOTH2001
81478-001-04PopCare100 in 1 BOTTLECLOTH1001
81478-001-05PopCare240 mL in 1 CONTAINERCLOTH2401
81478-001-05PopCare120 in 1 BOTTLECLOTH1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81478-001POPCARE (ISOPROPYL ALCOHOL) CLOTH [NINGBO THE ONE BIO-TECHNOLOGY CO., LTD]1Legacy NDC, 10 package rows20210129_b9e8de97-57fd-edc9-e053-2a95a90aff0f.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81478-00181478-001-01, 81478-001-02, 81478-001-03, 81478-001-04, 81478-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
b9e8df46-722a-34cd-e053-2a95a90a191bb9e8de97-57fd-edc9-e053-2a95a90aff0f2021-01-27WarningsExact identifier
spl id: b9e8df46-722a-34cd-e053-2a95a90a191b
spl set id: b9e8de97-57fd-edc9-e053-2a95a90aff0f

Reported adverse events (FAERS/openFDA)#

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