FDA.reportPublic FDA data

MEDeTATE

Manufacturer
DERMAdoctor, LLC | Total Nonsense
Effective date
2025-04-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:39:16

Label at a glance#

ProductMEDeTATE
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Dosage and administration

Apply to clean, dry underarm skin.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY 19%

Purpose

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces wetness due to stress

Warnings

WARNINGS SECTION

• For external use only

• Do not use on broken skin

• Stop use if rash or irritation occurs

• Ask a doctor before use if you have kidney disease

• Do not get into eyes

• Keep out of reach of children.

Directions

INSTRUCTIONS FOR USE SECTION

Apply to clean, dry underarm skin.

Other Ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Aqua (Water), Glycerin, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Gamma Aminobutyric Acid, Solanum Lycopersicum (Tomato) Extract, Gynostemma Pentaphyllum Extract, Panax Ginseng Root Extract, Portulaca Oleracea Extract, Butylene Glycol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

purpose section

OTC - PURPOSE SECTION

antiperspirant

administration

DOSAGE & ADMINISTRATION SECTION

apply to clean dry underarm skin

Principal Display Panel MEDeTATE 30 packettes of 3 ml - 0.1 oz wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDeTATE

antiperspirant wipes

30 packettes of 3 ml - 0.1 oz wipes

MEDeTATEMEDeTATE

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68715-311-012020-01-31C16284748780-19d75b9d0-a7bc-f424-e053-dadaa90a57ceMEDeTATE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68715-311-01MEDeTATE1 in 1 CARTONLIQUID13
68715-311-01MEDeTATE3 mL in 1 PACKETLIQUID33

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68715-31168715-311-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
PURSLANEM6S840WXG5IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
ALCOHOL3K9958V90MIACT
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
Dipeptide Diaminobutyroyl Benzylamide Diacetate38H206R00RIACT
.GAMMA.-AMINOBUTYRIC ACID2ACZ6IPC6IIACT
TOMATOZ4KHF2C175IACT
GYNOSTEMMA PENTAPHYLLUM LEAF5DWS84R85MIACT
ASIAN GINSENGCUQ3A77YXIIACT

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
MEDeTATEMEDETATEDERMAdoctor, LLC07af67ac-a07f-4c39-e054-00144ff88e882025-04-12WarningsExact identifier
ndc (package): 68715-311-01
ndc (product): 68715-311
ndc11 (package): 68715031101
spl id: 329d593c-f4aa-9799-e063-6394a90a26f4
spl set id: 07af67ac-a07f-4c39-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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