Prescription drug · NDA
Tretinoin Cream (Tretinoin) NDC 62032-417
Tretinoin 1 mg/g · Cream · Topical · Obagi Cosmeceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62032-417-20 | 6203204172062032041720 | 1 TUBE in 1 CARTON (62032-417-20) / 20 g in 1 TUBEMarketed from Jan 26, 1973 |
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)
- Tretinoin Cream
- Generic name (nonproprietary)
- tretinoin
- Active ingredients
- Tretinoin — 1 mg/g
- Dosage form
- Cream
- Route
- Topical
- Labeler
- Obagi Cosmeceuticals LLCNDC labeler code 62032
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 017340
- Marketing start
- Listing expires
- Other FDA classes
- Retinoids (Chemical structure)
- Identifiers
- Product ID 62032-417_c96be1f7-0c29-4bc7-ac51-c3da8b4788fbSPL ID c96be1f7-0c29-4bc7-ac51-c3da8b4788fbSPL set ID 745cc3ce-60b4-4479-a055-316817567949RxCUI 106302, 106303, 198300UNII 5688UTC01R
- Pharmacologic class
- Retinoid
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
N462032041720followed by a unit qualifier and the quantityPackage 62032-0417-20. 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)
INDICATIONS AND USAGE Tretinoin is indicated for topical application in the treatment of acne vulgaris. The safety and efficacy of the long-term use of this product in the treatment of other disorders have not been established.
Excerpt only. Read the full label for complete information.
About NDC 62032-417
- What is NDC 62032-417?
- 62032-417 is the product NDC for Tretinoin Cream (tretinoin), Tretinoin 1 mg/g cream, listed with the FDA by Obagi Cosmeceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Tretinoin Cream (Tretinoin).
- What is the active ingredient?
- Tretinoin.
- Who is the labeler?
- Obagi Cosmeceuticals LLC, NDC labeler code 62032. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Tretinoin Cream?
- 2 other product NDCs are listed under this name. See all Tretinoin Cream NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Tretinoin Cream products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Tretinoin Creamtretinoin | Tretinoin .25 mg/g | CreamTopical | Obagi Cosmeceuticals LLC | 62032-414 | 62032-0414-20 |
| Tretinoin Creamtretinoin | Tretinoin .5 mg/g | CreamTopical | Obagi Cosmeceuticals LLC | 62032-412 | 62032-0412-20 |
Other NDCs under NDA 017340
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Retin-Atretinoin | Tretinoin 1 mg/g | CreamTopical | Bausch Health US, LLC | 0187-5164 |
| Tretinoin | Tretinoin 1 mg/g | CreamTopical | Mylan Pharmaceuticals Inc. | 0378-8084 |