FDA.reportPublic FDA data

Ocean breeze scented hand sanitizer

Manufacturer
Jinhua Magic color Cosmetic Co., Ltd | Townley Inc.
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:57

Label at a glance#

ProductOcean breeze scented hand sanitizer 01
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient .............purpose

alcohol Denate: 70%(v/v)..... Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only-hands

keep out of eyes- avoid contact with broken skin.

Keep away from fire.

Stop use and ask a dosctor if irritation or radness develops

Do not inhale or ingest. If swallowed, get medical help or contact a poison control right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 8 use under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER(AQUA/EAU), PEG-40 HYDROGENATED CASTOR OIL, FRAGRANCE( PARFUM), ACRYLATES/ c10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE.

Questions?

OTC - QUESTIONS SECTION

1-212-779-0544 weekdays

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76743-005-0176743-005-0176743-005-0576743-005-0576743-005-0276743-005-0276743-005-0376743-005-0376743-005-0476743-005-04

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76743-005-012022-01-28C16284748780-1d6a99b39-405e-a426-e053-dadaa90af4c2DC0333TA, FZ2160TA, FZ2162TA, DC0334TA, PX0001TA( clear, Ocean breeze)
76743-005-022022-01-28C16284748780-1d6a99b39-405e-a426-e053-dadaa90af4c2DC0333TA, FZ2160TA, FZ2162TA, DC0334TA, PX0001TA( clear, Ocean breeze)
76743-005-032022-01-28C16284748780-1d6a99b39-405e-a426-e053-dadaa90af4c2DC0333TA, FZ2160TA, FZ2162TA, DC0334TA, PX0001TA( clear, Ocean breeze)
76743-005-042022-01-28C16284748780-1d6a99b39-405e-a426-e053-dadaa90af4c2DC0333TA, FZ2160TA, FZ2162TA, DC0334TA, PX0001TA( clear, Ocean breeze)
76743-005-052022-01-28C16284748780-1d6a99b39-405e-a426-e053-dadaa90af4c2DC0333TA, FZ2160TA, FZ2162TA, DC0334TA, PX0001TA( clear, Ocean breeze)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76743-005-01Ocean breeze scented hand sanitizer01236 mL in 1 BOTTLE, PLASTICGEL2361
76743-005-02Ocean breeze scented hand sanitizer01236 mL in 1 BOTTLE, PLASTICGEL2361
76743-005-03Ocean breeze scented hand sanitizer01236 mL in 1 BOTTLE, PLASTICGEL2361
76743-005-04Ocean breeze scented hand sanitizer01236 mL in 1 BOTTLE, PLASTICGEL2361
76743-005-05Ocean breeze scented hand sanitizer01236 mL in 1 BOTTLE, PLASTICGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76743-005OCEAN BREEZE SCENTED HAND SANITIZER 01 (ALOCHOL) GEL [JINHUA MAGIC COLOR COSMETIC CO., LTD]1Legacy NDC, 5 package rows20200617_a82fc342-474e-0663-e053-2995a90afb5f.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76743-00576743-005-01, 76743-005-02, 76743-005-03, 76743-005-04, 76743-005-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
OCEAN POUT23LSR23L76IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
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
a82faca8-b61d-51ed-e053-2995a90a263aa82fc342-474e-0663-e053-2995a90afb5f2020-06-16WarningsExact identifier
spl id: a82faca8-b61d-51ed-e053-2995a90a263a
spl set id: a82fc342-474e-0663-e053-2995a90afb5f

Reported adverse events (FAERS/openFDA)#

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