Over-the-counter drug · UNAPPROVED DRUG OTHER
Yobisin (Rehmannia root, angelica gigas root) NDC 72988-0012
Rhubarb 16.7 mg/1 + 10 more ingredients · Tablet · Oral · Lydia Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72988-0012-1 | 72988001201 | 20 TABLET in 1 PACKAGE (72988-0012-1)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)
- Yobisin
- Generic name (nonproprietary)
- rehmannia root, angelica gigas root
- Active ingredients
- Rhubarb — 16.7 mg/1Rehmannia glutinosa root — 416.7 mg/1Angelica gigas root — 416.7 mg/1Akebia stem — 416.7 mg/1Scutellaria baicalensis root — 250 mg/1Licorice — 125 mg/1Alisma plantago-aquatica root — 250 mg/1Forsythia suspensa fruit — 16.7 mg/1Plantago seed — 250 mg/1Ginger — 16.7 mg/1Chinese cinnamon — 16.7 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Lydia Co., Ltd.NDC labeler code 72988
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)
- Identifiers
- Product ID 72988-0012_0ca8ac22-aaac-9d25-e063-6294a90a4541SPL ID 0ca8ac22-aaac-9d25-e063-6294a90a4541SPL set ID 873ef769-6051-4914-e053-2a95a90a9edbUNII G280W4MW6E, 1BEM3U6LQQ, 32766B2FHX, 531B9G152H, 7J95K7ID2S, 61ZBX54883, 6DXR2088WL, P4793M1ES5, 9C60Y73166, C5529G5JPQ, WS4CQ062KM
- 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
N472988001201followed by a unit qualifier and the quantityPackage 72988-0012-01. 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 .
Indications (excerpt from the label)
adults: 3~6 tablets twice a day 7 to 14 years old: 2-3 tablets twice a day
Excerpt only. Read the full label for complete information.
About NDC 72988-0012
- What is NDC 72988-0012?
- 72988-0012 is the product NDC for Yobisin, Rhubarb 16.7 mg/1 + 10 more ingredients tablet, 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?
- Yobisin (Rehmannia root, angelica gigas root).
- What is the active ingredient?
- Rhubarb, Rehmannia glutinosa root, Angelica gigas root, Akebia stem, Scutellaria baicalensis root, Licorice, Alisma plantago-aquatica root, Forsythia suspensa fruit, Plantago seed, Ginger, Chinese cinnamon.
- 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 Yobisin?
- 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.