FDA.reportPublic FDA data

GLINT

Manufacturer
GLINT COSMETICS PRIVATE LIMITED
Effective date
2018-02-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:28

Label at a glance#

ProductGLINT First Aid
Active ingredientBACITRACIN ZINC
Label structure12 sections

Indications and uses

■ first aid to help prevent infection in minor ■ cuts ■ scrapes ■ burns

Dosage and administration

■ clean the affected area ■ apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily • may be covered with a sterile bandage

Label contents#

Full prescribing information#

Active Ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION

Bacitracin Zinc (equal to 500 bacitracin units)

Purpose

OTC - PURPOSE SECTION

First Aid Antibiotic

Uses

INDICATIONS & USAGE SECTION

■ first aid to help prevent infection in minor ■ cuts ■ scrapes ■ burns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ Not for opthalmic use Do not use ■ in the eyes ■ if you are allergic to any of the ingredients ■ over large areas of the body longer than 1 week unless directed by a doctor

Ask a doctor before use in case of

OTC - ASK DOCTOR SECTION

■ deep or puncture wounds

■ animal bites ■ serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ the condition persists or gets worse

■ a rash or other allergic reaction develops

Keep out of reach of children

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

■ clean the affected area

■ apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily •may be covered with a sterile bandage

Other Information

SPL UNCLASSIFIED SECTION

■ store at room temperature 15-30C (59-86F)

■ avoid excessive heat and humidity

Inactive Ingredients

INACTIVE INGREDIENT SECTION

hard paraffin, liquid paraffin, white soft paraffin, lanolin

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUG FACTSDRUG FACTS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1366116bacitracin zinc 500 UNT/GM Topical OintmentPSN1
1366116bacitracin zinc 0.5 UNT/MG Topical OintmentSCD1
1366116bacitracin zinc 500 UNT per GM Topical OintmentSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BACITRACIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71486-3035-22020-01-31C16284748780-19d75b9d0-3cd3-f424-e053-dadaa90a57ceDrug Facts
71486-3035-32020-01-31C16284748780-19d75b9d0-3cd3-f424-e053-dadaa90a57ceDrug Facts
71486-3035-42020-01-31C16284748780-19d75b9d0-3cd3-f424-e053-dadaa90a57ceDrug Facts
71486-3035-52020-01-31C16284748780-19d75b9d0-3cd3-f424-e053-dadaa90a57ceDrug Facts
71486-3035-62020-01-31C16284748780-19d75b9d0-3cd3-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71486-3035-2GLINTFirst Aid0.9 g in 1 PACKETOINTMENT0.91
71486-3035-3GLINTFirst Aid14 g in 1 TUBEOINTMENT141
71486-3035-4GLINTFirst Aid28 g in 1 TUBEOINTMENT281
71486-3035-5GLINTFirst Aid113 g in 1 TUBEOINTMENT1131
71486-3035-6GLINTFirst Aid425 g in 1 JAROINTMENT4251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71486-3035GLINT FIRST AID (BACITRACIN ZINC) OINTMENT [GLINT COSMETICS PRIVATE LIMITED]1Legacy NDC, 5 package rows20180211_64e1f3b7-cc15-24a3-e053-2a91aa0a4521.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71486-303571486-3035-2, 71486-3035-3, 71486-3035-4, 71486-3035-5, 71486-3035-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
PARAFFINI9O0E3H2ZEIACT
MINERAL OILT5L8T28FGPIACT
PETROLATUM4T6H12BN9UIACT
LANOLIN7EV65EAW6HIACT
BACITRACIN ZINC89Y4M234ESACTIM

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
64e1f3b7-cc16-24a3-e053-2a91aa0a452164e1f3b7-cc15-24a3-e053-2a91aa0a45212018-02-10WarningsExact identifier
spl id: 64e1f3b7-cc16-24a3-e053-2a91aa0a4521
spl set id: 64e1f3b7-cc15-24a3-e053-2a91aa0a4521

Reported adverse events (FAERS/openFDA)#

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