Over-the-counter drug · OTC MONOGRAPH DRUG

Acetaminophen (Extra strength pain relief) NDC 68071-5239

Acetaminophen 500 mg/1 · Tablet · Oral · NuCare Pharmaceuticals,Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)68071-5239Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-5239Add 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
68071-5239-36807152390330 TABLET in 1 BOTTLE (68071-5239-3)Marketed from Apr 13, 2020
68071-5239-56807152390545 TABLET in 1 BOTTLE (68071-5239-5)Marketed from Apr 13, 2020
68071-5239-96807152390990 TABLET in 1 BOTTLE (68071-5239-9)Marketed from Apr 13, 2020

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)
Acetaminophen
Generic name (nonproprietary)
extra strength pain relief
Active ingredients
Acetaminophen — 500 mg/1
Dosage form
Tablet
Route
Oral
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 007
Marketing start
Listing expires
Identifiers
Product ID 68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4SPL ID 2a95afd1-cd26-371c-e063-6294a90a97d4SPL set ID a32f346e-71d0-cc11-e053-2a95a90ae88cRxCUI 198440UNII 362O9ITL9DUPC 0368071523935

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468071523903 followed by a unit qualifier and the quantity

Package 68071-5239-03. 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 temporarily relieves minor aches and pains temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-5239

What is NDC 68071-5239?
68071-5239 is the product NDC for Acetaminophen (extra strength pain relief), Acetaminophen 500 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acetaminophen (Extra Strength Pain Relief).
What is the active ingredient?
Acetaminophen.
Who is the labeler?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acetaminophen?
228 other product NDCs are listed under this name. See all Acetaminophen 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 Acetaminophen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
acetaminophenAcetaminophen 650 mg/1Tablet, Film coated, Extended releaseOralAmazon.com Services LLC72288-15072288-0150-79
AcetaminophenAcetaminophen 10 mg/mLInjection, SolutionIntravenousSomerset Therapeutics, LLC70069-87170069-0871-10
AcetaminophenAcetaminophen 500 mg/1TabletOralWalgreens0363-981000363-9810-1000363-9810-2500363-9810-50+1 more
AcetaminophenAcetaminophen 500 mg/1TabletOralPUBLIX SUPERMARKETS, INC41415-17541415-0175-0541415-0175-10
AcetaminophenAcetaminophen 500 mg/1TabletOralFamily Dollar, Inc.55319-75155319-0751-24
AcetaminophenAcetaminophen 500 mg/1TabletOralMeijer Distribution Inc79481-078079481-0780-0179481-0780-0279481-0780-04
AcetaminophenAcetaminophen 500 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-413268788-4132-0168788-4132-0268788-4132-03+1 more
acetaminophenAcetaminophen 500 mg/1TabletOralUnit Dose Solutions, Inc.87441-00887441-0008-01
AcetaminophenAcetaminophen 160 mg/5mLSolutionOralAcetris Pharma Holdings, LLC52343-55552343-0555-12
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralGranules India Limited62207-89262207-0892-4962207-0892-51

All 229 Acetaminophen NDCs

Other NDCs under M 007

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

FDA NDC Directory listings under M 007
ProductStrengthForm · routeLabelerProduct NDC
Stool Softener Laxativedocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralUnited Natural Foods, Inc. dba UNFI41163-241
Milk Of Magnesiamagnesium hydroxideMagnesium hydroxide 1200 mg/15mLLiquidOralDOLGENCORP, INC.55910-649
Stool Softenerdocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralReliable 1 Laboratories LLC69618-086
Magnesium CitrateMagnesium citrate 1.745 g/29.6mLLiquidOralThe Kroger Co.30142-899
citromamagnesium citrateMagnesium citrate 1.745 g/29.6mLLiquidOralVi-Jon, LLC0869-0164
Magnesium CitrateMagnesium citrate 1.745 g/29.6mLSolutionOralPublix Super Markets, Inc.56062-264
Careonepsyllium huskPsyllium husk .52 g/1CapsuleOralFOODHOLD USA41520-907
Stool Softenerdocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralA-S Medication Solutions50090-7167
Sennosides, Docusate SodiumDocusate sodium 50 mg/1; Sennosides 8.6 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-0195
Magnesium CitrateMagnesium citrate 1.745 g/29.6mLSolutionOralPublix Super Markets, Inc.56062-266
Mineral oilMineral oil 100 mg/100mLOilOralP & L Development, LLC49580-0334
Purifi Hand Sanitizerbenzalkonium chlorideBenzalkonium chloride .13 g/100mLSolutionTopicalPurifi LLC80659-301
Stool Softener Laxativedocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralCARDINAL HEALTH 110, LLC. DBA LEADER 7000070000-0091
CareOne Milk of Magnesia Cherrymagnesium hydroxideMagnesium hydroxide 1200 mg/15mLLiquidOralRetail Business Services, LLC.72476-665
Stool Softener Laxative Extra Strengthdocusate sodiumDocusate sodium 250 mg/1Capsule, Liquid filledOralWALMART INC. (see also Equate)79903-073
Dulcolax Pink Stool Softenerdocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralChattem, Inc.41167-0281
Quality Choice Laxativesodium phosphate, dibasic, unspecified form and sodium phosphate, monobasic, unspecified formSodium phosphate, Dibasic, Unspecified form 7 g/118mL; Sodium phosphate, Monobasic, Unspecified form 19 g/118mLEnemaRectalChain Drug Marketing Association83324-292
Magnesium CitrateMagnesium citrate 1.745 g/29.6mLLiquidOralSTRATEGIC SOURCING SERVICES70677-1112
Stool Softenerdocusate sodiumDocusate sodium 100 mg/1Capsule, Liquid filledOralBryant Ranch Prepack72162-2255
Milk of Magnesia Concentratemagnesium hydroxideMagnesium hydroxide 2400 mg/10mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-0940

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