NDC codes

FDA NDC Directory
Product NDC (as listed)69367-174Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69367-0174Add 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 NDC11-digit (billing)PackageCopy
69367-174-0169367017401693670174011 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

N469367017401 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Hydroquinone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
hydroquinoneHydroquinone 40 mg/gCreamTopicalMarlex Pharmaceuticals, Inc.10135-72410135-0724-99

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in