NDC codes

FDA NDC Directory
Product NDC (as listed)47682-769Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47682-0769Add 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
47682-769-69476820769694768207696960 mL in 1 CARTON (47682-769-69)Marketed from Jul 1, 2026

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)
Green Guard Instydose Mucus Relief
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 200 mg/10mL
Dosage form
Liquid
Route
Oral
Labeler
Unifirst First Aid CorporationNDC labeler code 47682
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 008
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 47682-769_5b21bd13-d64a-6570-e063-6394a90a51e9SPL ID 5b21bd13-d64a-6570-e063-6394a90a51e9SPL set ID 5b21bd13-d649-6570-e063-6394a90a51e9RxCUI 310604UNII 495W7451VQUPC 0347682216993
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

N447682076969 followed by a unit qualifier and the quantity

Package 47682-0769-69. 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 Uses 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 47682-769

What is NDC 47682-769?
47682-769 is the product NDC for Green Guard Instydose Mucus Relief, Guaifenesin 200 mg/10mL liquid, listed with the FDA by Unifirst First Aid Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Green Guard Instydose Mucus Relief (Guaifenesin).
What is the active ingredient?
Guaifenesin.
Who is the labeler?
Unifirst First Aid Corporation, NDC labeler code 47682. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Green Guard Instydose Mucus Relief?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 008

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

FDA NDC Directory listings under M 008
ProductStrengthForm · routeLabelerProduct NDC
RITE AID Regular Strength Pink Bismuthbismuth subsalicylateBismuth subsalicylate 525 mg/30mLSuspensionOralRITE AID CORPORATION11822-7060
RITE AID Ultra Strnght Pink Bismuthbismuth subsalicylateBismuth subsalicylate 525 mg/15mLSuspensionOralRITE AID CORPORATION11822-7070
Medique Diotamebismuth subsalicylateBismuth subsalicylate 262 mg/1Tablet, ChewableOralUnifirst First Aid Corporation47682-210
FEVIA Diarrhea Controlbismuth subsalicylateBismuth subsalicylate 262 mg/1Capsule, Liquid filledOralVIVUNT PHARMA LLC82706-028
5-Symptom Digestive Reliefbismuth subsalicylateBismuth subsalicylate 262 mg/1TabletOralTARGET CORPORATION11673-880
Topcare Stomach Relief Original Strengthbismuth subsalicylateBismuth subsalicylate 262 mg/1TabletOralTopCo Associates, LLC76162-001
Stomach Reliefbismuth subsalicylateBismuth subsalicylate 525 mg/30mLLiquidOralFamily Dollar (FAMILY WELLNESS)55319-560
Pepto Bismol CHEWABLESbismuth subsalicylateBismuth subsalicylate 262 mg/1Tablet, ChewableOralProcter & Gamble Manufactura S de RL de CV58933-002
Percy Medicinebismuth subsalicylateBismuth subsalicylate 1050 mg/10mLLiquidOralMerrick Medicine Company, Inc0322-2222
Bismuth Subsalicylate Suspension Regular Strengthbismuth subsalicylateBismuth subsalicylate 525 mg/30mLSuspensionOralAptaPharma Inc.76281-557
Pepto Bismol CHEWABLESbismuth subsalicylateBismuth subsalicylate 262 mg/1Tablet, ChewableOralProcter & Gamble Manufactura S de RL de CV58933-011
Stomach Relief - Regular Strengthbismuth subsalicylateBismuth subsalicylate 525 mg/30mLLiquidOralAptaPharma Inc.76281-537
Stomach Reliefbismuth subsalicylateBismuth subsalicylate 262 mg/1TabletOralChain Drug Marketing Association, Inc.83324-060
Stomach Relief - Maximum Strengthbismuth subsalicylateBismuth subsalicylate 1050 mg/30mLLiquidOralAptaPharma Inc.76281-538
Pepto Bismol Chewsbismuth subsalicylateBismuth subsalicylate 262 mg/1Tablet, ChewableOralThe Procter & Gamble Manufacturing Company37000-996
Stomach Relief, Maximum Strengthbismuth subsalicylateBismuth subsalicylate 1050 mg/30mLSuspensionOralAptaPharma Inc.76281-558
CVS Stomach Reliefbismuth subsalicylateBismuth subsalicylate 262 mg/1TabletOralCVS51316-124
Quality Choice Ultra Strength Stomach Reliefbismuth subsalicylateBismuth subsalicylate 525 mg/15mLLiquidOralQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)83324-337
Pepto Bismol CHEWABLESbismuth subsalicylateBismuth subsalicylate 525 mg/21Tablet, ChewableOralProcter & Gamble Manufactura S de RL de CV58933-013
POCKET PEPTO Pepto Bismolbismuth subsalicylateBismuth subsalicylate 262 mg/1TabletOralProcter & Gamble Manufactura S de RL de CV58933-017

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