What is NDC 83071-020?

83071-020 is the product NDC for Dr.Jucre Rebirth Activating Toner, Betaine .001 g/100mL liquid, listed with the FDA by NATURECELL CO., LTD.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Dr.Jucre Rebirth Activating Toner (Betaine).

NATURECELL CO., LTD., NDC labeler code 83071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dr.Jucre Rebirth Activating Toner?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dr.Jucre Rebirth Activating Toner NDC 83071-020

NDC codes

FDA NDC Directory

Product NDC (as listed)83071-020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83071-0020Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
83071-020-02	83071002002	1 BOTTLE in 1 CARTON (83071-020-02) / 150 mL in 1 BOTTLE (83071-020-01)Marketed from Oct 1, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dr.Jucre Rebirth Activating Toner
Generic name (nonproprietary): betaine
Active ingredients: Betaine — .001 g/100mL
Dosage form: Liquid
Route: Topical
Labeler: NATURECELL CO., LTD.NDC labeler code 83071
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Oct 1, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Methylating Activity (Mechanism)
Identifiers: Product ID 83071-020_ff0ae282-1f6c-441a-a7dd-863b46931dc2SPL ID ff0ae282-1f6c-441a-a7dd-863b46931dc2SPL set ID 7f333594-d672-4259-83ae-5d591e620f0dUNII 3SCV180C9W
Pharmacologic class: Methylating Agent

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483071002002 followed by a unit qualifier and the quantity

Package 83071-0020-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 7, 2022.

Indications (excerpt from the label)

Uses ■ skin protectant

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83071-020

What is NDC 83071-020?: 83071-020 is the product NDC for Dr.Jucre Rebirth Activating Toner, Betaine .001 g/100mL liquid, listed with the FDA by NATURECELL CO., LTD.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dr.Jucre Rebirth Activating Toner (Betaine).
What is the active ingredient?: Betaine.
Who is the labeler?: NATURECELL CO., LTD., NDC labeler code 83071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dr.Jucre Rebirth Activating Toner?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Dr.Jucre Rebirth Activating Toner (Betaine) NDC 83071-020