NDC codes

FDA NDC Directory
Product NDC (as listed)61152-600Labeler and product segments. Claims need a package NDC.
Product NDC at billing width61152-0600Add 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
61152-600-59611520600596115206005959 mL in 1 BOTTLE, SPRAY (61152-600-59)Marketed from Jun 19, 2025

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)
Snorestop
Generic name (nonproprietary)
nux vomica, belladonna, hydrastis canadensis, kali bichromicum, teucrium marum, histaminum hydrochloricum, laurocerasus, cinchona, stramonium
Active ingredients
Prunus laurocerasus leaf — 10 [hp_X]/59mLCinchona bark — 10 [hp_X]/59mLStrychnos nux-vomica seed — 10 [hp_X]/59mLHydrastis canadensis whole — 10 [hp_X]/59mLAtropa belladonna — 10 [hp_X]/59mLHistamine dihydrochloride — 10 [hp_X]/59mLTeucrium marum — 10 [hp_X]/59mLDatura stramonium — 10 [hp_X]/59mLPotassium dichromate — 10 [hp_X]/59mL
Dosage form
Spray
Route
Oral
Labeler
Green Pharmaceuticals IncNDC labeler code 61152
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers
Product ID 61152-600_3cbe7366-0da4-dfc9-e063-6394a90addbdSPL ID 3cbe7366-0da4-dfc9-e063-6394a90addbdSPL set ID 37f4ea81-691f-597b-e063-6294a90a84bdUNII F26P2D4757, 292E43P4I9, 269XH13919, R763EBH88T, WQZ3G9PF0H, 3POA0Q644U, 10464S0TAA, G6W4F0V8Z3, T4423S18FM
Pharmacologic class
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

N461152060059 followed by a unit qualifier and the quantity

Package 61152-0600-59. 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: Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61152-600

What is NDC 61152-600?
61152-600 is the product NDC for Snorestop, Prunus laurocerasus leaf 10 [hp_X]/59mL + 8 more ingredients spray, listed with the FDA by Green Pharmaceuticals Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Snorestop (Nux vomica, Belladonna, Hydrastis canadensis, Kali bichromicum, Teucrium marum, Histaminum hydrochloricum, Laurocerasus, Cinchona, Stramonium).
What is the active ingredient?
Prunus laurocerasus leaf, Cinchona bark, Strychnos nux-vomica seed, Hydrastis canadensis whole, Atropa belladonna, Histamine dihydrochloride, Teucrium marum, Datura stramonium, Potassium dichromate.
Who is the labeler?
Green Pharmaceuticals Inc, NDC labeler code 61152. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Snorestop?
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.

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