Prescription drug · UNAPPROVED DRUG OTHER
Hydroquinone NDC 69367-174
Hydroquinone 40 mg/g · Cream · Topical · Westminster Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69367-174-01 | 6936701740169367017401 | 1 TUBE in 1 CARTON (69367-174-01) / 28.35 g in 1 TUBEMarketed from Apr 16, 2018 |
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)
- Hydroquinone
- Generic name (nonproprietary)
- hydroquinone
- Active ingredients
- Hydroquinone — 40 mg/g
- Dosage form
- Cream
- Route
- Topical
- Labeler
- Westminster Pharmaceuticals, LLCNDC labeler code 69367
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Other FDA classes
- Depigmenting Activity (Physiologic effect)Melanin Synthesis Inhibitors (Mechanism)
- Identifiers
- Product ID 69367-174_c975cd31-f562-40a2-ae14-f31a00c5164eSPL ID c975cd31-f562-40a2-ae14-f31a00c5164eSPL set ID dc72c0b2-4505-4dcf-8a69-889cd9f41693RxCUI 197795UNII XV74C1N1AE
- Pharmacologic class
- Melanin Synthesis Inhibitor
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
N469367017401followed by a unit qualifier and the quantityPackage 69367-0174-01. 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)
INDICATIONS AND USAGE HYDROQUINONE USP, 4% SKIN BLEACHING CREAM is indicated for the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.
Excerpt only. Read the full label for complete information.
About NDC 69367-174
- What is NDC 69367-174?
- 69367-174 is the product NDC for Hydroquinone, Hydroquinone 40 mg/g cream, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Hydroquinone.
- What is the active ingredient?
- Hydroquinone.
- Who is the labeler?
- Westminster Pharmaceuticals, LLC, NDC labeler code 69367. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hydroquinone?
- 1 other product NDC are listed under this name. See all Hydroquinone NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Hydroquinone products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| hydroquinone | Hydroquinone 40 mg/g | CreamTopical | Marlex Pharmaceuticals, Inc. | 10135-724 | 10135-0724-99 |