FDA.reportPublic FDA data

Edge

Manufacturer
Emilia Personal Care Inc.
Effective date
2021-11-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:32

Label at a glance#

ProductEdge Antiperspirant Deodorant - Glacier Fresh
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium

Tetrachlorohydrex GLY, 17.6%

OTC - PURPOSE SECTION

Purpose

Antiperspirant

INDICATIONS & USAGE SECTION

Uses •reduces underarm wetness

WARNINGS SECTION

Warnings

For external use only. Do not use on broken

skin. Ask a doctor before use if you have kidney

disease. Stop use if rash occurs. Keep out of reach of

children. If swallowed, get medical help or contact a Poison

Control Center right away.

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.

DOSAGE & ADMINISTRATION SECTION

Directions •apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients cyclopentasiloxane,

stearyl alcohol, PPG-14 butyl ether, C12-15 alkyl

benzoate, trihydroxystearin, phenyl trimethicone,

petrolatum, distarch phosphate, fragrance, talc,

ethylhexylglycerin, bisabolol, BHT.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42421-018-012023-06-15C16284748780-19d75b9d0-17c5-f424-e053-dadaa90a57ceEDGE ANTIPERSPIRANT DEODORANT GLACIER FRESH
42421-018-012023-01-30C16284748780-19d75b9d0-17c5-f424-e053-dadaa90a57ceEDGE ANTIPERSPIRANT DEODORANT GLACIER FRESH
42421-018-012021-11-03C16284748780-19d75b9d0-17c5-f424-e053-dadaa90a57ceEDGE ANTIPERSPIRANT DEODORANT GLACIER FRESH
42421-018-012020-01-31C16284748780-19d75b9d0-17c5-f424-e053-dadaa90a57ceEDGE ANTIPERSPIRANT DEODORANT GLACIER FRESH

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42421-01842421-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
TRIHYDROXYSTEARIN06YD7896S3IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
PETROLATUM4T6H12BN9UIACT
STARCH, CORNO8232NY3SJIACT
TALC7SEV7J4R1UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LEVOMENOL24WE03BX2TIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB

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
fe2d9e90-ba4f-0ffa-e053-6294a90a8633ce0e92a9-8391-4e00-aef5-e452f138f3c82023-06-15WarningsExact identifier
spl set id: ce0e92a9-8391-4e00-aef5-e452f138f3c8

Reported adverse events (FAERS/openFDA)#

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