Dr.Jucre Rebirth Activating Toner
Dr.Jucre Rebirth Activating Toner is an FDA drug label for the active ingredient BETAINE manufactured by NATURECELL 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 20221107.
- Generic name
- BETAINE
- Manufacturer
- NATURECELL CO., LTD.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83071-020
- Application
- N/A
- Label effective
- 20221107
About this product
Dr.Jucre Rebirth Activating Toner is an FDA-registered drug product whose active ingredient is BETAINE. It is labelled by NATURECELL CO., LTD. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83071-020, label effective 20221107. It is one of 3 FDA drug label records sharing the active ingredient BETAINE. 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 BETAINE are most often described in connection with: skin protectant. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses ■ skin protectant
Dosage & Administration
Directions ■ Apply an appropriate amount evenly on the skin.
Warnings
WARNINGS For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Refrain from using it on wounded areas. Keep out of reach of children.
More products with the same ingredient
BETAINEHow products containing BETAINE compare
FDA lists 3 drug label records with BETAINE 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 form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Cosette Pharmaceuticals, Inc. | 1 |
| — | — | NATURECELL CO., LTD. | 1 |
| — | — | Recordati Rare Diseases | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Dr.Jucre Rebirth Activating Toner used for?
Uses ■ skin protectant
Who makes Dr.Jucre Rebirth Activating Toner?
NATURECELL CO., LTD. is the labeler of record for Dr.Jucre Rebirth Activating Toner. 3 FDA label records share the active ingredient BETAINE, 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 Dr.Jucre Rebirth Activating Toner 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 Dr.Jucre Rebirth Activating Toner 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 BETAINE?
Yes. 3 FDA drug label records list BETAINE 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 Dr.Jucre Rebirth Activating Toner 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.