Active ingredient

Manufacturer
Guangzhou Oupeng Cosmetics Co., Ltd.
Effective date
2026-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
weekly-update
Hydrated at
2026-07-17 21:42:12

Label at a glance#

ProductVENROCK
Active ingredientUNDECYLENIC ACID
Label structure11 sections

Indications and uses

For the treatment of damaged nails Helps improve the appearance of nails Targeted nail recovery and deep care while you sleep

Dosage and administration

Thoroughly clean and dry the affected nail.Twist off the cap. Use the nail file to gently file down thickened areas to improve absorption. Apply a few drops of the treatment liquid directly onto the nail and let it dry slightly. Apply the nail patch over the treated nail to protect the area and lock in the formula. Use daily for best results.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 25%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of damaged nails
  • Helps improve the appearance of nails
  • Targeted nail recovery and deep care while you sleep

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • On broken or irritated skin.
  • On children under 2 years of age unless directed by a doctor.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes and mouth. In case of contact, rinse immediately with clean water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Redness, irritation, or allergic reactions occur.
  • Condition does not improve or worsens.

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

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Thoroughly clean and dry the affected nail.Twist off the cap.
  • Use the nail file to gently file down thickened areas to improve absorption.
  • Apply a few drops of the treatment liquid directly onto the nail and let it dry slightly.
  • Apply the nail patch over the treated nail to protect the area and lock in the formula.
  • Use daily for best results.

Other information

OTHER SAFETY INFORMATION

Store in a cool, dry place away from direct sunlight, and keep the cap tightly closed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AVENA SATIVA (OAT) BRAN EXTRACT, BUTYLENE GLYCOL, HYDROXYETHYLCELLULOSE, LACTOBIONIC ACID, OPHIOPOGON JAPONICUS ROOT EXTRACT, OPUNTIA DILLENII SEED OIL, PAEONIA ALBIFLORA ROOT EXTRACT, PARAHYDROXYACETOPHENONE, PHENOXYETHANOL, PROPYLENE GLYCOL, SACCHARIDE ISOMERATE, SCUTELLARIA BAICALENSIS ROOT EXTRACT, WATER.

Questions or comments?

OTC - QUESTIONS SECTION

934-935-7135 / rangelcervel824@gmail.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VENROCK
NAIL RENEWAL SYSTEM
FOR DAMAGED NAILS
25% UNDECYLENIC ACID
PRECISION BRUSH APPLICATOR
OVERNIGHT NAIL PATCHES
CLINICALLY INSPIRED CARE
1 FL. OZ. (30ml)

Packaging DesignPackaging Design

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85772-000985772-0009-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
VENROCKUNDECYLENIC ACIDGuangzhou Oupeng Cosmetics Co., Ltd.558af06e-6fe1-c926-e063-6394a90a738c2026-07-01WarningsExact identifier
ndc (package): 85772-0009-1
ndc (product): 85772-0009
ndc11 (package): 85772000901
spl id: 558af06e-6fe2-c926-e063-6394a90a738c
spl set id: 558af06e-6fe1-c926-e063-6394a90a738c

Reported adverse events (FAERS/openFDA)#

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