What is NDC 11673-436?

11673-436 is the product NDC for Jock Itch Cream (butenafine hydrochloride), Butenafine hydrochloride 10 mg/g cream, listed with the FDA by TARGET CORPORATION. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Jock Itch Cream (Butenafine Hydrochloride).

TARGET CORPORATION, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Jock Itch Cream?

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.

Jock Itch Cream NDC 11673-436 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)11673-436Labeler and product segments. Claims need a package NDC.

Product NDC at billing width11673-0436Add 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
11673-436-01	1167304360111673043601	1 TUBE in 1 CARTON (11673-436-01) / 12 g in 1 TUBEMarketed from Nov 15, 2024

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): Jock Itch Cream
Generic name (nonproprietary): butenafine hydrochloride
Active ingredients: Butenafine hydrochloride — 10 mg/g
Dosage form: Cream
Route: Topical
Labeler: TARGET CORPORATIONNDC labeler code 11673
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205181
Marketing start: Nov 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Benzylamines (Chemical structure)
Identifiers: Product ID 11673-436_3909394c-0658-e681-e063-6394a90a5e04SPL ID 3909394c-0658-e681-e063-6394a90a5e04SPL set ID 1d8a17ae-4e25-f591-e063-6394a90a35ddRxCUI 1298448UNII R8XA2029ZIUPC 0311673436011
Pharmacologic class: Benzylamine Antifungal

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

N411673043601 followed by a unit qualifier and the quantity

Package 11673-0436-01. 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 3, 2025.

Indications (excerpt from the label)

Uses cures most jock itch relieves itching, burning, crackling, and scaling which accompany this condition

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11673-436

What is NDC 11673-436?: 11673-436 is the product NDC for Jock Itch Cream (butenafine hydrochloride), Butenafine hydrochloride 10 mg/g cream, listed with the FDA by TARGET CORPORATION. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Jock Itch Cream (Butenafine Hydrochloride).
What is the active ingredient?: Butenafine hydrochloride.
Who is the labeler?: TARGET CORPORATION, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Jock Itch Cream?: 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 205181

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

FDA NDC Directory listings under ANDA 205181
Product	Strength	Form · route	Labeler	Product NDC
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Walgreen Company	0363-2100
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Target Corporation	11673-016
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Rite Aid Corporation	11822-2100
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	TOPCO ASSOCIATES LLC	36800-049
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-2100
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	CVS Pharmacy	69842-986
Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	STRATEGIC SOURCING SERVICES LLC	70677-1269
Athletes Foot Ultrabutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	H E B	37808-013
Athletes Foot Ultrabutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Wal-Mart Stores Inc	49035-225
Butenafine Hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Albertsons	21130-965
Butenafine Hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	YYBA CORP	73581-210
Butenafine Hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	MEIJER DISTRIBUTION INC	79481-0086
Butenafine Hydrochloride 1%butenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	CVS Pharmacy	69842-989
Butenafine Hydrochloride Athletes Footbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Kroger Company	30142-210
Butenafine Hydrochloride Jock Itchbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Wal-Mart Stores Inc	49035-178
Jock Itchbutenafine hydrochloride	Butenafine hydrochloride 10 mg/g	CreamTopical	Walgreen Company	0363-2101

Jock Itch Cream (Butenafine hydrochloride) NDC 11673-436