Snore Control NDC 57955-9983

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9983Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9983Add 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 NDC	11-digit (billing)	Package	Copy
57955-9983-2	57955998302	59 mL in 1 BOTTLE, SPRAY (57955-9983-2)Marketed from Mar 15, 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): Snore Control
Generic name (nonproprietary): bromium, chamomilla, cinchona, cuprum metallicum, helleborus niger, histaminum hydrochloricum, hydrastis canadensis, kali bichromicum, laurocerasus, nux vomica, phosphoricum acidum, rhus tox, silicea, stramonium, sulphur and zincum metallicum.
Active ingredients: Bromine — 10 [hp_X]/59mLMatricaria chamomilla whole — 10 [hp_X]/59mLCinchona officinalis bark — 10 [hp_X]/59mLCopper — 10 [hp_X]/59mLHelleborus niger root — 10 [hp_X]/59mLHistamine dihydrochloride — 10 [hp_X]/59mLGoldenseal — 10 [hp_X]/59mLPotassium dichromate — 10 [hp_X]/59mLPrunus laurocerasus leaf — 10 [hp_X]/59mLStrychnos nux-vomica seed — 10 [hp_X]/59mLPhosphoric acid — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLSilicon dioxide — 10 [hp_X]/59mLDatura stramonium — 10 [hp_X]/59mLSulfur — 10 [hp_X]/59mLZinc — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 57955-9983_6f361b61-60c1-4c90-8121-59b1a47c2197SPL ID 6f361b61-60c1-4c90-8121-59b1a47c2197SPL set ID 704bb574-6c54-49d1-bdae-81ffe0e79d10UNII SBV4XY874G, G0R4UBI2ZZ, S003A158SB, 789U1901C5, 608DGJ6815, 3POA0Q644U, ZW3Z11D0JV, T4423S18FM, F26P2D4757, 269XH13919, E4GA8884NN, 6IO182RP7A, ETJ7Z6XBU4, G6W4F0V8Z3, 70FD1KFU70, J41CSQ7QDS
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Plant Allergenic Extract

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

N457955998302 followed by a unit qualifier and the quantity

Package 57955-9983-02. 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 Mar 4, 2026.

Indications (excerpt from the label)

Uses † For temporary relief of symptoms related to snoring: slow, labored breathing stuffy nose, especially at night heaviness of chest dry cough † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)