What is NDC 77052-010?

77052-010 is the product NDC for Ala-Scalp (hydrocortisone), Hydrocortisone 20 mg/mL lotion, listed with the FDA by Derm Ventures LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Derm Ventures LLC, NDC labeler code 77052. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ala-Scalp?

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.

Ala-Scalp NDC 77052-010 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)77052-010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width77052-0010Add 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 NDC	11-digit (billing)	Package	Copy
77052-010-01	77052001001	1 BOTTLE, WITH APPLICATOR in 1 BOX (77052-010-01) / 29.6 mL in 1 BOTTLE, WITH APPLICATORMarketed from Jan 1, 2021
77052-010-02	77052001002	1 BOTTLE, WITH APPLICATOR in 1 BOX (77052-010-02) / 59.2 mL in 1 BOTTLE, WITH APPLICATORMarketed from Jul 24, 2020

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): Ala-Scalp
Generic name (nonproprietary): hydrocortisone
Active ingredients: Hydrocortisone — 20 mg/mL
Dosage form: Lotion
Route: Topical
Labeler: Derm Ventures LLCNDC labeler code 77052
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 083231
Marketing start: Jul 24, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 77052-010_561ef342-40b0-ab51-e063-6394a90a5747SPL ID 561ef342-40b0-ab51-e063-6394a90a5747SPL set ID 61498a40-3b3c-4066-89c8-d99686e2d638RxCUI 197784, 884077UNII WI4X0X7BPJUPC 0377052010029
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

N477052001001 followed by a unit qualifier and the quantity

Package 77052-0010-01. 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 Jul 8, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrocortisone Lotion is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 77052-010

What is NDC 77052-010?: 77052-010 is the product NDC for Ala-Scalp (hydrocortisone), Hydrocortisone 20 mg/mL lotion, listed with the FDA by Derm Ventures LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ala-Scalp (Hydrocortisone).
What is the active ingredient?: Hydrocortisone.
Who is the labeler?: Derm Ventures LLC, NDC labeler code 77052. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ala-Scalp?: 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 ANDA 083231

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 083231
Product	Strength	Form · route	Labeler	Product NDC
Hydrocortisonehydrocortisone lotion	Hydrocortisone 20 mg/mL	LotionTopical	Allegis Holdings LLC	71297-010

Ala-Scalp (Hydrocortisone) NDC 77052-010