NDC codes

FDA NDC Directory
Product NDC (as listed)0573-2871Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00573-2871Add 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
0573-2871-0400573287104005732871042 CARTON in 1 PACKAGE (0573-2871-04) / 1 TUBE in 1 CARTON / 57 g in 1 TUBEMarketed from Mar 1, 2004
0573-2871-1000573287110005732871101 TUBE in 1 CARTON (0573-2871-10) / 28 g in 1 TUBEMarketed from Mar 1, 2004
0573-2871-2000573287120005732871201 TUBE in 1 CARTON (0573-2871-20) / 57 g in 1 TUBEMarketed from Mar 1, 2004
0573-2871-9100573287191005732871911 TUBE in 1 CARTON (0573-2871-91) / 28 g in 1 TUBEMarketed from Mar 1, 2018
0573-2871-9200573287192005732871921 TUBE in 1 CARTON (0573-2871-92) / 57 g in 1 TUBEMarketed from Mar 1, 2018
0573-2871-9300573287193005732871931 TUBE in 1 CARTON (0573-2871-93) / 28 g in 1 TUBEMarketed from Jun 1, 2019
0573-2871-9400573287194005732871941 TUBE in 1 CARTON (0573-2871-94) / 57 g in 1 TUBEMarketed from May 17, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Preparation H
Generic name (nonproprietary)
mineral oil, petrolatum, phenylephrine hcl
Active ingredients
Phenylephrine hydrochloride — 2.5 mg/gMineral oil — 140 mg/gPetrolatum — 749 mg/g
Dosage form
Ointment
Route
Topical
Labeler
Haleon US Holdings LLCNDC labeler code 0573
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 015
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha1-Agonists (Mechanism)
Identifiers
Product ID 0573-2871_128ba16d-dbb2-1073-e063-6394a90a8ba6SPL ID 128ba16d-dbb2-1073-e063-6394a90a8ba6SPL set ID 507c08ab-a98b-33fe-e2ac-eb9b9a810d5aRxCUI 1372298UNII 04JA59TNSJ, T5L8T28FGP, 4T6H12BN9U
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 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

N400573287104 followed by a unit qualifier and the quantity

Package 00573-2871-04. 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)

USES helps relieve the local itching and discomfort associated with hemorrhoids temporarily shrinks hemorrhoidal tissue and relieves burning temporarily provides a coating for relief of anorectal discomforts temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0573-2871

What is NDC 0573-2871?
0573-2871 is the product NDC for Preparation H, Phenylephrine hydrochloride 2.5 mg/g + 2 more ingredients ointment, listed with the FDA by Haleon US Holdings LLC. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Preparation H (Mineral oil, petrolatum, phenylephrine HCl).
What is the active ingredient?
Phenylephrine hydrochloride, Mineral oil, Petrolatum.
Who is the labeler?
Haleon US Holdings LLC, NDC labeler code 0573. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Preparation H?
5 other product NDCs are listed under this name. See all Preparation H 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 Preparation H NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Preparation Hphenylephrine hydrochloridePhenylephrine hydrochloride 6.25 mg/1SuppositoryRectalHaleon US Holdings LLC0573-291900573-2919-1200573-2919-2400573-2919-48
Preparation Hphenylephrine hydrochloridePhenylephrine hydrochloride 6.25 mg/1SuppositoryRectalHaleon US Holdings LLC0573-137800573-1378-0000573-1378-0100573-1378-06
Preparation Hcocoa butter, phenylephrine hydrochloride, and witch hazel—KitHaleon US Holdings LLC0573-288400573-2884-12
Preparation Hcocoa butter, phenylephrine hydrochlorideCocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.25 mg/1SuppositoryRectalHaleon US Holdings LLC0573-2880—
Preparation Hcocoa butter, phenylephrine hydrochlorideCocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.25 mg/1SuppositoryRectalHaleon US Holdings LLC0573-2883—

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
ProductStrengthForm · routeLabelerProduct NDC
Pramoxine Hydrochloride Anorectalpramoxine hydrochloridePramoxine hydrochloride 1 mg/mLLotionTopicalStratus Pharmaceuticals58980-522
Ma Ying Long Musk Hemorrhoidspetrolatum, zinc oxidePetrolatum 779.9 mg/g; Zinc oxide 76 mg/gOintmentTopicalMayinglong Pharmaceutical Group Co., Ltd.68511-997
Mayinglong Hemorrhoidalpetrolatum, zinc oxidePetrolatum 779.9 mg/g; Zinc oxide 76 mg/gOintmentTopicalMayinglong Pharmaceutical Group Co., Ltd.68511-998
hemorrhoidal maximum strength pain reliefglycerin, phenylephrine hcl, pramoxine hcl, white petrolatumGlycerin 14.4 g/100g + 3 more ingredientsCreamTopicalKroger Company30142-944
Preparation Hcocoa butter, phenylephrine hydrochloride, and witch hazel—KitHaleon US Holdings LLC0573-2884
Hemorrhoidalmineral oil, petrolatum, phenylephrine hclMineral oil 14 g/100g + 2 more ingredientsOintmentRectalKroger Company30142-188
rexall hemorrhoidalcocoa butter, phenylephrine hclCocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1SuppositoryRectalDolgencorp Inc55910-279
Witch HazelWitch hazel 860 mg/mLLiquidTopicalCVS Pharmacy, Inc.59779-045
Dermatool Hemorrhoidalglycerin, lidocaine, petrolatum, phenylephrine hclLidocaine 5 g/100g + 3 more ingredientsCreamTopicalPapalo Group LLC84728-413
Acolye Numbing Cream Anorectal(Hemorrhoidal) CreamlidocaineLidocaine 5 g/100gCreamTopicalGuangzhou Haishi Biological Technology Co., Ltd.60771-0028
Hemorrhoid Anestheticmineral oil, petrolatum, phenylephrine hclPetrolatum .749 g/g + 2 more ingredientsOintmentTopicalSavvy Care and Cosmetics83650-110
hemorrhoidalcocoa butter, phenylephrine hclCocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1SuppositoryRectalMeijer Distribution Inc41250-279
Lidocaine Numbing CreamlidocaineLidocaine .05 g/gCreamTopicalShanghai Chuangshi Medical Technology (Group) Co., Ltd.73557-311
RWWXII Deep Numbing Cream(Anorectal Hemorrhoidal Cream)lidocaineLidocaine 5 g/100gCreamTopicalGuangzhou Haishi Biological Technology Co., Ltd.60771-0027
Barrier Protectant Creambarrier creamMenthol 1 mg/g; Zinc oxide 200 mg/gOintmentTopicalCardinal Health63517-003
ER Hemorrhoidphenylephrine hclMineral oil .14 g/g + 2 more ingredientsCreamRectalEVER READY FIRST AID72976-018
ANIXIKE Numbinglidocaine4% numbingLidocaine 4 g/100gCreamTopicalJiangxi Yudexi Pharmaceutical Co., LTD85248-166
Meijer Maximum strength pain relieving cleansingbenzalkonium chloride and lidocaine hydrochlorideBenzalkonium chloride .13 g/100mL; Lidocaine hydrochloride 4 g/100mLLiquidTopicalMEIJER DISTRIBUTION, INC.41250-287
hemorrhoidalglycerin, phenylephrine hcl, pramoxine hcl, white petrolatumGlycerin 14.4 g/100g + 3 more ingredientsCreamTopicalMeijer Distribution Inc41250-944
Equaline Hemorrhoidalcocoa butter, phenylephrine hclCocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1SuppositoryRectalUnited Natural Foods, Inc. dba UNFI41163-279

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