NDC codes

FDA NDC Directory
Product NDC (as listed)17856-1248Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17856-1248Add 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
17856-1248-11785612480117856124801100 POUCH in 1 BOX, UNIT-DOSE (17856-1248-1) / 1 TABLET, FILM COATED in 1 POUCHMarketed from May 9, 2024

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

Generic name (nonproprietary)
docusate sodium 50 mg and sennosides 8.6 mg
Active ingredients
Sennosides — 8.6 mg/1Docusate sodium — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M
Marketing start
Listing expires
Identifiers
Product ID 17856-1248_38930b8a-9e76-2025-e063-6394a90a2478SPL ID 38930b8a-9e76-2025-e063-6394a90a2478SPL set ID 4c02fcec-6bb7-4497-96c5-0d809209dd17RxCUI 998740UNII 3FYP5M0IJX, F05Q2T2JA0

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

N417856124801 followed by a unit qualifier and the quantity

Package 17856-1248-01. 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 .

Indications (excerpt from the label)

Uses relieves occasional constipation (irregularity) generally produces a bowel movement in 6 to 12 hours

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-1248

What is NDC 17856-1248?
17856-1248 is the product NDC for Stimulant Laxative Plus Stool Softener, Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 tablet, film coated, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Stimulant Laxative Plus Stool Softener (Docusate Sodium 50 mg and Sennosides 8.6 mg).
What is the active ingredient?
Sennosides, Docusate sodium.
Who is the labeler?
ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Stimulant Laxative Plus Stool Softener?
4 other product NDCs are listed under this name. See all Stimulant Laxative Plus Stool Softener 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 Stimulant Laxative Plus Stool Softener NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Stimulant Laxative Plus Stool Softenerdocusate sodium and sennosidesSennosides 8.6 mg/1; Docusate sodium 50 mg/1Tablet, Film coatedOralGOOD SENSE50804-30450804-0304-10
Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mgSennosides 8.6 mg/1; Docusate sodium 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-767468788-7674-0168788-7674-06
Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mgSennosides 8.6 mg/1; Docusate sodium 50 mg/1Tablet, Film coatedOralRUGBY LABORATORIES0536-124800536-1248-0100536-1248-10
Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mgSennosides 8.6 mg/1; Docusate sodium 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-269371335-2693-0171335-2693-0271335-2693-03+6 more

Other NDCs under M

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

FDA NDC Directory listings under M
ProductStrengthForm · routeLabelerProduct NDC
Ab 3000benzalkonium chlorideBenzalkonium chloride .13 kg/100kgLiquidTopicalChemco63039-1006
Adult Low Dose AspirinaspirinAspirin 81 mg/1Tablet, Delayed releaseOralPharbest Pharmaceuticals, Inc.16103-356
Alcoholisopropyl alcoholIsopropyl alcohol .7 g/gSwabTopicalHART Health50332-0046
Alcoholisopropyl alcoholIsopropyl alcohol 70 mL/100mLSprayTopicalNorMed50332-0213
Alcoholisopropyl alcoholIsopropyl alcohol 70 mL/100mLSprayTopicalNorMed50332-0223
Aluminum HydroxideAluminum hydroxide 320 mg/5mLLiquidOralATLANTIC BIOLOGICALS CORP.17856-0091
Antibacterial Handsoapbenzalkonium chlorideBenzalkonium chloride .13 g/.1LLiquidTopicalChemcor Chemical Corporation68041-604
Antibacterial Liquid Handbenzalkonium chlorideBenzalkonium chloride 13 kg/100kgLiquidTopicalMorgan Gallacher Inc. DBA Custom Chemical Formulators Inc.50241-317
Anua Zero-Cast Moisturizing Finish Sunscreen SPF 50avobenzone, homosalate, octisalate, octocryleneAvobenzone 30 mg/mL + 3 more ingredientsLotionTopicalENGLEWOOD LAB, INC.14268-169
AspirinAspirin 325 mg/1TabletOralHART Health50332-0139
Aspirin Low Dose Chewable OrangeaspirinAspirin 81 mg/1Tablet, ChewableOralATLANTIC BIOLOGICALS CORP.17856-6794
Bandagebenzocaine and benzethonium chlorideBenzethonium chloride 170 mg/85g; Benzocaine 2720 mg/85gAerosol, SprayTopicalHART Health50332-0218
Blood Clottingbenzethonium chloride and lidocaineLidocaine 3400 mg/85g; Benzethonium chloride 170 mg/85gAerosol, SprayTopicalHART Health50332-0217
Bonica EaseX Pain Relievingcamphor (synthetic), menthol, methyl salicylateCamphor (Synthetic) 31 mg/g + 2 more ingredientsPatchTopicalPlanet (Anhui) Pharmaceutical Co., Ltd.75568-036
Broncochem Cold And Flu Teaacetaminophen-phenylephrine hydrochloride-chlorpheniramine maleateAcetaminophen 500 mg/13g; Chlorpheniramine maleate 4 mg/13gGranule, For solutionOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-097
Broncochem Expectorant IIacetaminophen-chlorpheniramine maleate-dextromethorphan hbr-guaifenesin-phenylephrine hclAcetaminophen 325 mg/10mL + 3 more ingredientsSyrupOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-011
Broncochem Kids Cold And Fluacetaminophen-phenylephrine hcl-guaifenesinAcetaminophen 325 mg/10mL + 2 more ingredientsSyrupOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-109
Broncochem Maximum Coughdextromethorphan hbr-gyaifenesinDextromethorphan hydrobromide 20 mg/10mL; Guaifenesin 400 mg/10mLSyrupOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-100
Broncochem Maximum Cough Kidsdextromethorphan hbr-guaifenesinDextromethorphan hydrobromide 10 mg/15mL; Guaifenesin 100 mg/15mLSyrupOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-180
Broncochem Maximum Cough Nightdextromethorphan hbr-pyrilamine maleateDextromethorphan hydrobromide 15 mg/5mL; Pyrilamine maleate 6 mg/5mLSyrupOralLABORATORIO MAGNACHEM INTERNATIONAL SRL65131-035

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