What is NDC 82442-060?

82442-060 is the product NDC for up and up (phenylephrine hydrochloride), Phenylephrine hydrochloride 6.25 mg/1 suppository, 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?

up and up (Phenylephrine hydrochloride).

Target Corporation, NDC labeler code 82442. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for up and up?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

up and up NDC 82442-060 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82442-060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82442-0060Add 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
82442-060-12	82442006012	12 BLISTER PACK in 1 CARTON (82442-060-12) / 1 SUPPOSITORY in 1 BLISTER PACKMarketed from Aug 3, 2026

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): up and up
Generic name (nonproprietary): phenylephrine hydrochloride
Active ingredients: Phenylephrine hydrochloride — 6.25 mg/1
Dosage form: Suppository
Route: Rectal
Labeler: Target CorporationNDC labeler code 82442
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 015
Marketing start: Aug 3, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha1-Agonists (Mechanism)
Identifiers: Product ID 82442-060_57c2c6b9-a8fa-a1c6-e063-6294a90a97e5SPL ID 57c2c6b9-a8fa-a1c6-e063-6294a90a97e5SPL set ID b42775ae-44fe-487e-b9ca-21d9687020a9RxCUI 2715398UNII 04JA59TNSJ
Pharmacologic class: alpha-1 Adrenergic Agonist

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N482442006012 followed by a unit qualifier and the quantity

Package 82442-0060-12. 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 29, 2026.

Indications (excerpt from the label)

Uses helps relieve the local itching and discomfort associated with hemorrhoids temporarily shrinks hemorrhoidal tissue temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82442-060

What is NDC 82442-060?: 82442-060 is the product NDC for up and up (phenylephrine hydrochloride), Phenylephrine hydrochloride 6.25 mg/1 suppository, 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?: up and up (Phenylephrine hydrochloride).
What is the active ingredient?: Phenylephrine hydrochloride.
Who is the labeler?: Target Corporation, NDC labeler code 82442. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for up and up?: 1 other product NDC are listed under this name. See all up and up 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 up and up NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
UP and UPbenzalkonium chloride	Benzalkonium chloride 130 mg/100mL	LiquidTopical	TARGET CORPORATION INC.	82442-088	82442-0088-07

Other NDCs under M 015

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

FDA NDC Directory listings under M 015
Product	Strength	Form · route	Labeler	Product NDC
0.25 % PHENYLEPHRINE HCl HEMORRHOIDALmineral oil, petrolatum, phenylephrine hydrochloride	Mineral oil 14 g/100g + 2 more ingredients	OintmentTopical	Nantong Health & Beyond Hygienic Products Inc.	43473-094
0.25 % PHENYLEPHRINE HCl HEMORRHOIDALmineral oil, petrolatum, phenylephrine hydrochloride	Mineral oil 14 g/100g + 2 more ingredients	OintmentTopical	Universal Distribution Center LLC	52000-438
5% Lidocaine 10g5% lidocaine	Lidocaine 5 g/100g	CreamTopical	Chongqing Mandongzi Technology Co., Ltd	88002-001
Acolye Numbing Cream Anorectal(Hemorrhoidal) Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangzhou Haishi Biological Technology Co., Ltd.	60771-0028
Acolye Numbing Cream Anorectal(Hemorrhoidal) Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangzhou Haishi Biological Technology Co., Ltd.	60771-0029
Acolye Numbing Cream Anorectal(Hemorrhoidal) Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangdong Aimu Biological Technology Co., Ltd	83566-615
Adellina Lidocaine Numbing Cream Anorectal(Hemorrhoidal) Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangzhou Haishi Biological Technology Co., Ltd.	60771-0041
Adellina Lidocaine Numbing Cream Topical Anorectal Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangdong Aimu Biological Technology Co., Ltd	83566-612
Adellina Lidocaine Numbing Cream Topical Anorectal Creamlidocaine	Lidocaine 5 g/100g	CreamTopical	Guangdong Aimu Biological Technology Co., Ltd	83566-614
ADVANCED NUMB Topical Anestheticlidocaine hydrochloride	Lidocaine hydrochloride 50 mg/g	CreamTopical	Uber Scientific, LLC	71131-052
AER Pre-moistened Witch Hazel Padwitch hazel	Witch hazel 500 mg/mL	SolutionRectal, Topical	Birchwood Laboratories LLC	50289-3250
AER Traveler Toweletteaer traveler	Witch hazel .5 g/1	SolutionRectal, Topical	Birchwood Laboratories LLC	50289-4200
Americainebenzocaine	Benzocaine 5.6 g/28g	OintmentTopical	Insight Pharmaceuticals LLC	63736-375
AnievaLClidocaine	Lidocaine .05 g/g	CreamTopical	Blackstone Products, LLC	87798-001
ANIXIKE Numbinglidocaine4% numbing	Lidocaine 4 g/100g	CreamTopical	Jiangxi Yudexi Pharmaceutical Co., LTD	85248-166
Arlun LIDOCAINE Creamlidocaine cream	Lidocaine 5 g/100g	CreamTopical	Guangzhou Jingliang Cosmetics Co., Ltd.	87408-021
Assured Bikini Smooth Creamlidocaine	Lidocaine 2 g/100g	CreamTopical	Zhejiang Jingwei Pharmaceutical Co., Ltd.	55621-011
Asteroidmenthol, petrolatum, zinc oxide	Menthol .098 g/28g + 2 more ingredients	OintmentTopical	HEALTHTEX LIMITED	84107-552
B-SURE Traveler Toweletteb-sure traveler	Witch hazel .5 g/g	SolutionRectal, Topical	Birchwood Laboratories LLC	50289-9250
Barrier Protectant Creambarrier cream	Menthol 1 mg/g; Zinc oxide 200 mg/g	OintmentTopical	Cardinal Health	63517-003

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up and up (Phenylephrine hydrochloride) NDC 82442-060

NDC codes

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About NDC 82442-060

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About NDC 82442-060

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Other NDCs under M 015