ORALINE-SECURE ANTIPERSPIRANT 2 OZ

Manufacturer
NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.
Effective date
2025-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:52:51

Label at a glance#

ProductORALINE-SECURE ANTIPERSPIRANT 2 OZ
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Dosage and administration

Apply thin layer to underam.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM CHLOROHYDRATE 10% w/w

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Helps lessen underarm perspiration.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease.

Keep out of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply thin layer to underam.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua,dipropylene Glycol,peg-40 Hydrogenated Castor Oil, Polysorbate 20, Parfum, Hydroxyethylcellulose, Phenoxyethanol, Menthol, Disodium EDTA

84641-005-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84641-002-0184641-002-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84641-005-01ORALINE-SECURE ANTIPERSPIRANT 2 OZ288 in 1 BOXLIQUID2881
84641-005-01ORALINE-SECURE ANTIPERSPIRANT 2 OZ56.7 g in 1 TUBE, WITH APPLICATORLIQUID56.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84641-005ORALINE-SECURE ANTIPERSPIRANT 2 OZ (ALUMINUM CHLOROHYDRATE) LIQUID [NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.]12 package rows20250117_2bcd888f-8207-7e64-e063-6394a90a1687.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84641-00584641-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
2bcd888f-8208-7e64-e063-6394a90a16872bcd888f-8207-7e64-e063-6394a90a16872025-01-16WarningsExact identifier
spl id: 2bcd888f-8208-7e64-e063-6394a90a1687
spl set id: 2bcd888f-8207-7e64-e063-6394a90a1687

Reported adverse events (FAERS/openFDA)#

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