FDA.reportPublic FDA data

Face Saver Gel

Manufacturer
Tripak Pharmaceuticals
Effective date
2023-11-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:58:41

Label at a glance#

ProductFace Saver Gel
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 82309-024-04 Label 50 gLabel 50 g

OTC - ACTIVE INGREDIENT SECTION

Aluminium Zirconium Tetrachlorhydrex Gly 16% Antiperspirant

OTC - PURPOSE SECTION

Uses:

decreases perspiration

reduces wetness

WARNINGS SECTION

For external use only

INDICATIONS & USAGE SECTION

Do not use:

-on broken skin - on an area that is infected or reddened


When using this product
• do not use in or near eyes •apply to facial area only


Stop use and ask a doctor if
• rash, irritation or sensitivity develops
Ask a doctor before use if you have kidney disease

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
• Shake well before use • Apply a dab to the palms of the hands, apply sparingly •Apply to the face •Product can be applied daily

For daily use place a dab on hand and apply

OTHER SAFETY INFORMATION


Other information
• Store at below 30 °C(86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Propylene Glycol, Cydopentasiloxane, Cyclotetrasiloxane, PEG/PPG-18/18 Dimethicone, Fragrance

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82309-024-042025-01-30C16284748780-12cef2736-78e4-d83d-e063-dadaa90ab31fFace Saver Gel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82309-024FACE SAVER GEL (ANTIPERSPIRANT) GEL [TRIPAK PHARMACEUTICALS]2Legacy NDC20231102_d0ec9eef-e014-e377-e053-2995a90a4cbf.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
82309-02482309-024-04

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
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
WATER059QF0KO0RIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOMETHICONE 4CZ227117JEIACT

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
091fc02c-5c36-d72a-e063-6294a90aa920d0ec9eef-e014-e377-e053-2995a90a4cbf2023-11-01WarningsExact identifier
spl id: 091fc02c-5c36-d72a-e063-6294a90aa920
spl set id: d0ec9eef-e014-e377-e053-2995a90a4cbf