Clobetasol Propionate (emollient) NDC 72162-2628

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2628Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2628Add 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
72162-2628-2	72162262802	1 TUBE in 1 CARTON (72162-2628-2) / 15 g in 1 TUBEMarketed from Apr 23, 2026
72162-2628-3	72162262803	1 TUBE in 1 CARTON (72162-2628-3) / 30 g in 1 TUBEMarketed from Apr 23, 2026
72162-2628-6	72162262806	1 TUBE in 1 CARTON (72162-2628-6) / 60 g in 1 TUBEMarketed from Apr 23, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Clobetasol Propionate (emollient)
Generic name (nonproprietary): clobetasol propionate
Active ingredients: Clobetasol propionate — .5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209411
Marketing start: Sep 29, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 72162-2628_99405b91-475b-4174-a989-9954e763d2dfSPL ID 99405b91-475b-4174-a989-9954e763d2dfSPL set ID cb0bc057-d6ab-4eea-af7a-01661ae9b517RxCUI 1992281UNII 779619577M
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

N472162262802 followed by a unit qualifier and the quantity

Package 72162-2628-02. 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 Apr 23, 2026.

Indications (excerpt from the label)

Clobetasol propionate cream USP, 0.05% (emollient) is a corticosteroid indicated for: The relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 12 years of age or older. (1.1) The treatment of moderate to severe plaque-type psoriasis in patients 16 years of age and older. (1.2) Limitations of Use Clobetasol propionate cream USP, 0.05% (emollient) should not be used in the treatment of rosacea or perioral dermatitis, and should not be used on the face, groin, or axillae. (1.3) The total dosage should not exceed 50 grams per week. (1.3) Avoid use if skin atrophy is present at the treatment site. (1.3) Clobetasol propionate cream USP, 0.05% (…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209411

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

FDA NDC Directory listings under ANDA 209411
Product	Strength	Form · route	Labeler	Product NDC
Clobetasol Propionate (emollient)clobetasol propionate	Clobetasol propionate .5 mg/g	CreamTopical	The J. Molner Company LLC	83148-064