THE SKINHOUSE VITA SNAIL FIRST ESSENSE

NIACINAMIDE, ADENOSINE TOPICAL HUMAN OTC DRUG

THE SKINHOUSE VITA SNAIL FIRST ESSENSE is an FDA drug label for the active ingredient NIACINAMIDE, ADENOSINE manufactured by NOKSIBCHO cosmetic Co., Ltd. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20210715.

Generic name
NIACINAMIDE, ADENOSINE
Manufacturer
NOKSIBCHO cosmetic Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
73590-0082
Application
N/A
Label effective
20210715

About this product

THE SKINHOUSE VITA SNAIL FIRST ESSENSE is an FDA-registered drug product whose active ingredient is NIACINAMIDE, ADENOSINE. It is labelled by NOKSIBCHO cosmetic Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73590-0082, label effective 20210715. It is one of 23 FDA drug label records sharing the active ingredient NIACINAMIDE, ADENOSINE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing NIACINAMIDE, ADENOSINE are most often described in connection with: smoothes skin, effectively prepares, care routines. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENT NIACINAMIDE 2.0% ADENOSINE 0.04%

Indications & Usage

Uses ■ It refreshes and smoothes skin and effectively prepares the next skin care routines.

Dosage & Administration

Directions ■ Use in the morning and at night after cleansing.

Warnings

WARNINGS For external use only. Avoid contact with eyes. Keep out of reach of children. Discontinue use if signs of irritation appear.

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How products containing NIACINAMIDE, ADENOSINE compare

FDA lists 23 drug label records with NIACINAMIDE, ADENOSINE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — LAON COMMERCE co ltd 10
— — NOKSIBCHO cosmetic Co., Ltd. 7
— — HANSCOS Co.,Ltd. 4
— — inthismorning co ltd 2
— — — —

Frequently asked questions

What is THE SKINHOUSE VITA SNAIL FIRST ESSENSE used for?
Uses ■ It refreshes and smoothes skin and effectively prepares the next skin care routines.

Who makes THE SKINHOUSE VITA SNAIL FIRST ESSENSE?
NOKSIBCHO cosmetic Co., Ltd. is the labeler of record for THE SKINHOUSE VITA SNAIL FIRST ESSENSE. 23 FDA label records share the active ingredient NIACINAMIDE, ADENOSINE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does THE SKINHOUSE VITA SNAIL FIRST ESSENSE come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is THE SKINHOUSE VITA SNAIL FIRST ESSENSE prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing NIACINAMIDE, ADENOSINE?
Yes. 23 FDA drug label records list NIACINAMIDE, ADENOSINE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has THE SKINHOUSE VITA SNAIL FIRST ESSENSE been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.