87066-5912

Manufacturer
Hubei Redrui Building Materials Co., Ltd. | Yiwu Ruishi E Commerce Co.Ltd | Guangzhou Yishenghe Traditional Chinese Medicine Technology Co., Ltd.
Effective date
2026-03-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:51:33

Label at a glance#

Product87066-5912
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

Apply to underarms only. clean and dry skin before use. spray an appropriate amount and rub until absorbed. use 1-2 times daily

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

  • Reduces underarm wetness

Warnings

WARNINGS SECTION

  • For external use only

Do not use

OTC - DO NOT USE SECTION

  • On broken skin. if you are allergic to alcohol

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • Kidney disease

When using this product

OTC - WHEN USING SECTION

  • Do not get into eyes. If product gets into eyes, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Rash or irritation occurs

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only. clean and dry skin before use. spray an appropriate amount and rub until absorbed. use 1-2 times daily

Other information

OTHER SAFETY INFORMATION

  • It is normal for a small amount of raw material to precipitate after long-term storage, which does not affect normal use. Store in a cool, dry place away from direct

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, ALCOHOL, PROPYLENE GLYCOL, GLYCERIN, PEG-40 HYDROGENATED CASTOR OIL, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER, HYDROXYETHYLCELLULOSE, FRAGRANCE FLORAL, POPULUS TREMULOIDES BARK, CETRIMONIUM BROMIDE, ALOE BARBADENSIS LEAF JUICE, PROPANEDIOL, 1,2-BUTANEDIOL, PHENOXYETHANOL, HYDROXYACETOPHENONE, CROCUS SATIVUS FLOWER, POLYSORBATE 60, DISODIUM PHOSPHATE, CYNANCHUM VINCETOXICUM LEAF, SODIUM PHOSPHATE, SILVER CATION

Questions or comments?

OTC - QUESTIONS SECTION

934-935-7135 / Rangelcervel824@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ELIMINATE BODY ODOR. (Eliminate Body Odor. Reduce Body Odor.) (The spring breeze for ten miles is not as good as you, fortunately Xinting found you.) packaging labelspackaging labels

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87066-5912-187066-59121 g in 1 CARTONSPRAY12

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87066-591287066-5912-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
87066-5912ALUMINUM CHLOROHYDRATE SPRAYHubei Redrui Building Materials Co., Ltd.3e960c2b-c365-d837-e063-6394a90a78762026-03-25WarningsExact identifier
ndc (package): 87066-5912-1
ndc (product): 87066-5912
ndc11 (package): 87066591201
spl id: 4de4b3b3-661b-ba8f-e063-6394a90a6a43
spl set id: 3e960c2b-c365-d837-e063-6394a90a7876

Reported adverse events (FAERS/openFDA)#

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