FDA.reportPublic FDA data

Dr. Nona

Manufacturer
Emilia Cosmetics Ltd
Effective date
2020-01-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:46:40

Label at a glance#

ProductDr. Nona
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure12 sections

Storage and handling

Storage : Store in a cool, dry and dark place with lid tightly closed.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY 15%

OTC - PURPOSE SECTION

Purpose

Antiperspirant

INDICATIONS & USAGE SECTION

Use  -reduces underarm wetness

WARNINGS SECTION

Warnings  -for external use only

Do not use on broken skin.

Ask doctor before use if you have kidney disease

Stop use if rash or irritation occurs

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, sterayl alcohol, PPG-

14 butyl ether, C12-15 alkyl benzoate, hydrogenated castor oil,

fragrance, steareth-21, ricinus communis (castor) seed oil, hydrogenated castor oil, copernicia cerifera (carnauba)

wax, silica, PEG-8 distearate, behenyl alcohol, BHT, maris sal (dead sea mineral

water), alpha isomethylionone, benyl salicylate, citronellol, courmarin,

hydroxyisohexyl-3-cyclohexene carboxaldehyde, limonene, linalool

STORAGE AND HANDLING SECTION

Storage: Store in a cool, dry and dark place with lid tightly closed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43219-001-172023-06-17C16284748780-1f386c649-cacf-0266-e053-dadaa90a7c1aecf2056b-f0c2-496c-8e14-9adfa2ddcc7a
43219-001-182023-06-17C16284748780-1f386c649-cacf-0266-e053-dadaa90a7c1aecf2056b-f0c2-496c-8e14-9adfa2ddcc7a
43219-001-172023-01-30C16284748780-1f386c649-cacf-0266-e053-dadaa90a7c1aecf2056b-f0c2-496c-8e14-9adfa2ddcc7a
43219-001-182023-01-30C16284748780-1f386c649-cacf-0266-e053-dadaa90a7c1aecf2056b-f0c2-496c-8e14-9adfa2ddcc7a

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43219-00143219-001-17, 43219-001-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
STEARETH-2153J3F32P58IACT
CASTOR OILD5340Y2I9GIACT
CARNAUBA WAXR12CBM0EIZIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PEG-8 DISTEARATE7JNC8VN07MIACT
DOCOSANOL9G1OE216XYIACT
TALC7SEV7J4R1UIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
WATER059QF0KO0RIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
CITRONELLA OILQYO8Q067D0IACT
COUMARINA4VZ22K1WTIACT
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDEQUE43B9Z2QIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB

Source Document#

Source XML · Source PDF

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
fe530208-597d-71e5-e053-6394a90ac98becf2056b-f0c2-496c-8e14-9adfa2ddcc7a2023-06-17WarningsExact identifier
spl set id: ecf2056b-f0c2-496c-8e14-9adfa2ddcc7a

Reported adverse events (FAERS/openFDA)#

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