NDC codes

FDA NDC Directory
Product NDC (as listed)70677-1013Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70677-1013Add 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
70677-1013-170677101301706771013014 BLISTER PACK in 1 CARTON (70677-1013-1) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Apr 13, 2023
70677-1013-27067710130270677101302500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70677-1013-2)Marketed from Mar 4, 2026
70677-1013-370677101303706771013032 BLISTER PACK in 1 BOX (70677-1013-3) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Sep 9, 2026

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)
Foster and Thrive Mucus Relief
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 600 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Strategic Sourcing Services LLCNDC labeler code 70677
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209215
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 70677-1013_510298d7-b70c-48f8-931b-683600379163SPL ID 510298d7-b70c-48f8-931b-683600379163SPL set ID f4ab5611-8abb-4c1f-8f85-917e2e1328e3RxCUI 636522UNII 495W7451VQ
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

N470677101301 followed by a unit qualifier and the quantity

Package 70677-1013-01. 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)

USE(S) helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70677-1013

What is NDC 70677-1013?
70677-1013 is the product NDC for Foster and Thrive Mucus Relief (guaifenesin), Guaifenesin 600 mg/1 tablet, extended release, listed with the FDA by Strategic Sourcing Services LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Foster and Thrive Mucus Relief (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
Strategic Sourcing Services LLC, NDC labeler code 70677. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Foster and Thrive Mucus Relief?
1 other product NDC are listed under this name. See all Foster and Thrive Mucus Relief 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 Foster and Thrive Mucus Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
foster and thrive mucus reliefguaifenesinGuaifenesin 600 mg/1Tablet, Multilayer, Extended releaseOralStrategic Sourcing Services LLC70677-129170677-1291-01

Other NDCs under ANDA 209215

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

FDA NDC Directory listings under ANDA 209215
ProductStrengthForm · routeLabelerProduct NDC
Equate Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralWal-Mart Stores, Inc.49035-284
GuaifenesinGuaifenesin 600 mg/1TabletOralYYBA CORP73581-400
Guaifenesin Extended Release 600 mgguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralWal-Mart Stores, Inc.79903-271
Guaifenesin Extended-Release 1200 mgguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralGuardian Drug Company53041-234
Guaifenesin Extended-Release 600 mgguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGuardian Drug Company53041-233
Maximum Strength Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralStrategic Sourcing Services LLC70677-1320
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8637
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-6986
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralDiscount Drug Mart, Inc53943-233
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralMcKesson Corporation dba SKY Packaging63739-067
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2642
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-499
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralYYBA Corp73581-403
Mucus Relief 600 mgguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGuardian Drug Company53041-190
Mucus Relief MaxguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralDiscount Drug Mart, Inc53943-234
Mucus Relief Maximum Strength 1200 mgguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralGuardian Drug Company53041-191
Topco Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralTopco Associates, LLC36800-226

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