What is NDC 72988-0011?

72988-0011 is the product NDC for Baenosin, Licorice .5 g/1 + 5 more ingredients capsule, listed with the FDA by Lydia Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Baenosin (Platycodon root, licorice, jujube, peony root).

What is the active ingredient?

Licorice, Paeonia lactiflora root, Platycodon grandiflorum root, Jujube fruit, Ginger, Poncirus trifoliata fruit.

Lydia Co., Ltd., NDC labeler code 72988. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Baenosin?

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.

Baenosin NDC 72988-0011 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72988-0011Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72988-0011Add 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
72988-0011-1	72988001101	10 CAPSULE in 1 PACKAGE (72988-0011-1)Marketed from Apr 24, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Baenosin
Generic name (nonproprietary): platycodon root, licorice, jujube, peony root
Active ingredients: Licorice — .5 g/1Paeonia lactiflora root — .5 g/1Platycodon grandiflorum root — .67 g/1Jujube fruit — .5 g/1Ginger — .5 g/1Poncirus trifoliata fruit — .5 g/1
Dosage form: Capsule
Route: Oral
Labeler: Lydia Co., Ltd.NDC labeler code 72988
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Apr 22, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 72988-0011_0ca8ac22-aaab-9d25-e063-6294a90a4541SPL ID 0ca8ac22-aaab-9d25-e063-6294a90a4541SPL set ID 874f9b81-80eb-05fd-e053-2a95a90afdebUNII 61ZBX54883, 3Z3866YW6P, 2DF0NS0O2Z, G55HNL2C70, C5529G5JPQ, 44445L49J2
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472988001101 followed by a unit qualifier and the quantity

Package 72988-0011-01. 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 Dec 16, 2023.

Indications (excerpt from the label)

adults take 2 capsules 3 times a day before meals or between meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72988-0011

What is NDC 72988-0011?: 72988-0011 is the product NDC for Baenosin, Licorice .5 g/1 + 5 more ingredients capsule, listed with the FDA by Lydia Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Baenosin (Platycodon root, licorice, jujube, peony root).
What is the active ingredient?: Licorice, Paeonia lactiflora root, Platycodon grandiflorum root, Jujube fruit, Ginger, Poncirus trifoliata fruit.
Who is the labeler?: Lydia Co., Ltd., NDC labeler code 72988. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Baenosin?: 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.