NDC codes

FDA NDC Directory
Product NDC (as listed)69842-732Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69842-0732Add 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
69842-732-146984207321414 BLISTER PACK in 1 CARTON (69842-732-14) / 1 TABLET in 1 BLISTER PACKMarketed from Feb 28, 2019
69842-732-286984207322828 BLISTER PACK in 1 CARTON (69842-732-28) / 1 TABLET in 1 BLISTER PACKMarketed from Feb 28, 2019
69842-732-426984207324242 BLISTER PACK in 1 CARTON (69842-732-42) / 1 TABLET in 1 BLISTER PACKMarketed from Feb 28, 2019

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)
Mucus Relief Extended Release Maximum StrengthSuffix: Maximum Strength
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 1200 mg/1
Dosage form
Tablet
Route
Oral
Labeler
CVS PharmacyNDC labeler code 69842
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207342
Marketing start
Marketing end
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 69842-732_0cc1967b-b883-486b-9a4f-519e1579a986SPL ID 0cc1967b-b883-486b-9a4f-519e1579a986SPL set ID 34314503-b253-4b44-96ff-a42fe2bb161fRxCUI 310621UNII 495W7451VQUPC 0050428072653
Pharmacologic class
Expectorant

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

N469842073214 followed by a unit qualifier and the quantity

Package 69842-0732-14. 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 loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and makes coughs more productive.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69842-732

What is NDC 69842-732?
69842-732 is the product NDC for Mucus Relief Extended Release Maximum Strength, Guaifenesin 1200 mg/1 tablet, listed with the FDA by CVS Pharmacy. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Mucus Relief Extended Release Maximum Strength (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
CVS Pharmacy, NDC labeler code 69842. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mucus Relief Extended Release Maximum Strength?
3 other product NDCs are listed under this name. See all Mucus Relief Extended Release Maximum Strength 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 Mucus Relief Extended Release Maximum Strength NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralH E B37808-76237808-0762-1437808-0762-42
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCARDINAL HEALTH 110, LLC. DBA LEADER 7000070000-047970000-0479-0170000-0479-02
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralWalgreens0363-083200363-0832-1400363-0832-28

Other NDCs under ANDA 207342

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

FDA NDC Directory listings under ANDA 207342
ProductStrengthForm · routeLabelerProduct NDC
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralH E B37808-762
Mucus Relief Extended Release Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCARDINAL HEALTH 110, LLC. DBA LEADER 7000070000-0479
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralRugby Laboratories0536-1392
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralBest Choice (Valu Merchandisers Company)63941-731
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralH E B37808-830
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralFamily Dollar (FAMILY WELLNESS)55319-733
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1052
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralH E B37808-935
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralRite Aid Corporation11822-3252
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralHarris Teeter, LLC69256-731
Mucus Relief ERguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralCardinal Health 107, LLC55154-4153
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 1200 mg/1TabletOralTARGET Corporation11673-732
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 600 mg/1TabletOralCare One (American Sales Company)41520-731
Mucus Relief Maximum StrengthguaifenesinGuaifenesin 1200 mg/1TabletOralCare One (American Sales Company)41520-732
Mucus Relief Extended ReleaseguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralRugby Laboratories, Inc.0536-1163
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1051
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralWinCo Foods, LLC67091-370
GuaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAmneal Pharmaceuticals LLC65162-036
GuaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralAmneal Pharmaceuticals LLC65162-037
Mucus ReliefguaifenesinGuaifenesin 600 mg/1TabletOralDolgencorp, Inc. (DOLLAR GENERAL & REXALL)55910-739

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