FDA.reportPublic FDA data

VENROCK

Manufacturer
Guangzhou Oupeng Cosmetics Co., Ltd. | Guangzhou Meihui International Biotechnology Co., Ltd.
Effective date
2025-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:05:48

Label at a glance#

ProductVENROCK
Active ingredientALUMINUM CHLOROHYDRATE
Label structure11 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

For external use on armpits only. Take an appropriate amount of this product and spray evenly on the armpits. Use daily after bathing for best results.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 10%

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

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 contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Rash or irritation develops and persists.

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

  • For external use on armpits only.
  • Take an appropriate amount of this product and spray evenly on the armpits.
  • Use daily after bathing for best results.

Other information

OTHER SAFETY INFORMATION

Store in a cool, dry place. Avoid direct sunlight and high temperatures. Seal the container tightly after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, BUTYLENE GLYCOL, PROPYLENE GLYCOL, PEG-40 HYDROGENATED CASTOR OIL, ETHYLHEXYLGLYCERIN, LEONTOPODIUM ALPINUM EXTRACT, METHYLPARABEN, DISODIUM EDTA, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, STEPHANIA TETRANDRA ROOT EXTRACT, CAPRYLHYDROXAMIC ACID, GENTIANA SCABRA EXTRACT, PARFUM

Questions or comments?

OTC - QUESTIONS SECTION

934-935-7135 / Yiqinzhi726@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VENROCK
BODY ODOR PURIFYING WATER
The smell is fragrant and fresh Antiperspirant
1.18 fl.oz / 35 ml
VENROCK BODY ODOR PURIFYING WATERVENROCK BODY ODOR PURIFYING WATER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85772-0003-1VENROCK1 g in 1 CARTONSPRAY11

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85772-000385772-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEONTOPODIUM ALPINUM7R4LQP52DMIACT
PIPER METHYSTICUM ROOTBOW48C81XPIACT
STEPHANIA TETRANDRA ROOT48PS81XHK0IACT
1,3-BUTYLENE GLYCOL 1-PROPIONATE17U77WTV66IACT
GENTIANA SCABRA ROOTGXZ33VNT92IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIPROPYLENE GLYCOLE107L85C40IACT
METHYLPARABENA2I8C7HI9TIACT
CALCIUM DISODIUM EDTA8U5D034955IACT
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
FRAGRANCE 135765EM498GW35IACT
AQUA059QF0KO0RIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT

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
VENROCKALUMINUM CHLOROHYDRATE SPRAYGuangzhou Oupeng Cosmetics Co., Ltd.3862d1b8-d4b1-480c-e063-6394a90a78ea2025-06-25WarningsExact identifier
ndc (package): 85772-0003-1
ndc (product): 85772-0003
ndc11 (package): 85772000301
spl id: 3862d1b8-d4b2-480c-e063-6394a90a78ea
spl set id: 3862d1b8-d4b1-480c-e063-6394a90a78ea

Reported adverse events (FAERS/openFDA)#

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