MICRO-INFUSION SYSTEM

Manufacturer
Ningbo Kenwei International Trade Co., Ltd.
Effective date
2026-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:11

Label at a glance#

ProductMICRO INFUSIONSYSTEM
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Eye protection: Avoid getting shampoo foam into your baby's eyes during washing. If it accidentally gets into their eyes, gently rinse with clean water until the irritation subsides. Skin reaction: If persistent redness, itching, or blistering occurs, discontinue use and consult a pediatrician. Storage and handling: Keep out of reach of children, store in a cool, dark place, and avoid direct sunlight and high temperatures. Use within the expiration date indicated on the packaging after opening.

INDICATIONS & USAGE SECTION

Deep Dermal Hydration: Restores skin elasticity to reduce new marks.
Collagen Support: Boosts fibroblast activity to repair stretch-related skin trauma.
Skin Soothing: Calms redness and irritation on stretched or damaged skin.
Pigment Softening: Helps fade the color of both red and white stretch marks.
Barrier Repair: Strengthens skin and supports stretch mark recovery.

WARNINGS SECTION

For external use only. Keep out of reach of children. Discontinue if irritation occurs. Used for those over 18 years old Storage condition: Do not store above 30°C (86°F). It is recommended to store it in a cool and dry place, avoiding direct sunlight.

INACTIVE INGREDIENT SECTION

1,2-Pentanediol

Sodium Chloride

Water

Octanoyl Hydroxamic Acid

RECENT MAJOR CHANGES SECTION

Deep Dermal Hydration: Restores skin elasticity to reduce new marks.
Collagen Support: Boosts fibroblast activity to repair stretch-related skin trauma.
Skin Soothing: Calms redness and irritation on stretched or damaged skin.
Pigment Softening: Helps fade the color of both red and white stretch marks.
Barrier Repair: Strengthens skin and supports stretch mark recovery.

OTC - PURPOSE SECTION

Deep Dermal Hydration: Restores skin elasticity to reduce new marks.
Collagen Support: Boosts fibroblast activity to repair stretch-related skin trauma.
Skin Soothing: Calms redness and irritation on stretched or damaged skin.
Pigment Softening: Helps fade the color of both red and white stretch marks.
Barrier Repair: Strengthens skin and supports stretch mark recovery.

DOSAGE & ADMINISTRATION SECTION

Direction 1. Unscrew the serum vial and fill the Infusion device with the serum. 2. Twist on the needle head securely. 3. Turn the device upside down for 1-2 minutes to allow serum flow. 4. Gently stamp the device across areas affected by stretch marks (e.g. stomach, hips, thighs, arms, breasts). 5. Apply any remaining serum to the treated area.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87640-001-01MICRO INFUSIONSYSTEM20 mL in 1 BOTTLELIQUID201

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87640-00187640-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4ACTIB

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
MICRO INFUSIONSYSTEMSEEK GLONingbo Kenwei International Trade Co., Ltd.50746cab-bfcc-fe0b-e063-6394a90adc012026-04-27WarningsExact identifier
ndc (package): 87640-001-01
ndc (product): 87640-001
ndc11 (package): 87640000101
spl id: 5074615f-3623-7b3b-e063-6294a90a39c7
spl set id: 50746cab-bfcc-fe0b-e063-6394a90adc01

Reported adverse events (FAERS/openFDA)#

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