UNTRA DRY ANTI-PERSPIRANT and DEODORANT -COOL BLAST

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2016-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:57:22

Label at a glance#

ProductUNTRA DRY ANTI-PERSPIRANT and DEODORANT -COOL BLAST
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Dosage and administration

remove cap, turn dial to raise product, apply envely to underarms only, replace cap after use.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrates 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness and perspiration.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken or irritated skin.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Posion Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

remove cap, turn dial to raise product, apply envely to underarms only, replace cap after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral Oil, Stearic Acid, Stearyl Alcohol, Cyclopentasiloxane, Isopropyl Palmitate, Hydrogenated Castor Oil, Fragrance, Silica, PEG-8 Distearate, BHT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-03676176-036-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
6cedc0c4-6d62-db32-e053-2991aa0a72f66cedc0c4-6d6d-db32-e053-2991aa0a72f62016-01-01WarningsExact identifier
spl id: 6cedc0c4-6d62-db32-e053-2991aa0a72f6
spl set id: 6cedc0c4-6d6d-db32-e053-2991aa0a72f6

Reported adverse events (FAERS/openFDA)#

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