Over-the-counter drug · OTC MONOGRAPH DRUG
Dermoscribe Seborrheic Dermatitis (Sulfur, salicylic acid, hydrocortisone) NDC 69683-202
Sulfur 3 g/100g + 2 more ingredients · Cream · Topical · DERMOSCRIBE PTY LTD
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69683-202-11 | 6968302021169683020211 | 60 g in 1 BOTTLE (69683-202-11)Marketed from Mar 23, 2015 |
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)
- Dermoscribe Seborrheic Dermatitis
- Generic name (nonproprietary)
- sulfur, salicylic acid, hydrocortisone
- Active ingredients
- Sulfur — 3 g/100gSalicylic acid — 3 g/100gHydrocortisone — 1 g/100g
- Dosage form
- Cream
- Route
- Topical
- Labeler
- DERMOSCRIBE PTY LTDNDC labeler code 69683
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 032
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 69683-202_4161aee0-5f36-1739-e063-6294a90a5bdfSPL ID 4161aee0-5f36-1739-e063-6294a90a5bdfSPL set ID 2b6bf90b-5d42-4c08-afee-56e13122285eRxCUI 1738574UNII 70FD1KFU70, O414PZ4LPZ, WI4X0X7BPJ
- Pharmacologic class
- Corticosteroid
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
N469683020211followed by a unit qualifier and the quantityPackage 69683-0202-11. 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)
USE For relief of itching, scaling, redness, flaking and irritation associated with seborrheic dermatitis
Excerpt only. Read the full label for complete information.
About NDC 69683-202
- What is NDC 69683-202?
- 69683-202 is the product NDC for Dermoscribe Seborrheic Dermatitis, Sulfur 3 g/100g + 2 more ingredients cream, listed with the FDA by DERMOSCRIBE PTY LTD. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Dermoscribe Seborrheic Dermatitis (Sulfur, Salicylic acid, Hydrocortisone).
- What is the active ingredient?
- Sulfur, Salicylic acid, Hydrocortisone.
- Who is the labeler?
- DERMOSCRIBE PTY LTD, NDC labeler code 69683. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Dermoscribe Seborrheic Dermatitis?
- 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.
Other NDCs under M 032
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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