Snorestop

Product NDC
61152-600
11-digit product format
611520600
Labeler code
61152
Product ID
61152-600_3cbe7366-0da4-dfc9-e063-6394a90addbd
Type
HUMAN OTC DRUG
Nonproprietary name
Nux vomica, Belladonna, Hydrastis canadensis, Kali bichromicum, Teucrium marum, Histaminum hydrochloricum, Laurocerasus, Cinchona, Stramonium
Dosage form
SPRAY
Route
ORAL
Labeler
Green Pharmaceuticals Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-06-19
Substance
ATROPA BELLADONNA; CINCHONA BARK; DATURA STRAMONIUM; HISTAMINE DIHYDROCHLORIDE; HYDRASTIS CANADENSIS WHOLE; POTASSIUM DICHROMATE; PRUNUS LAUROCERASUS LEAF; STRYCHNOS NUX-VOMICA SEED; TEUCRIUM MARUM
Active strength
10; 10; 10; 10; 10; 10; 10; 10; 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Snorestop
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PRUNUS LAUROCERASUS LEAF10 [hp_X]/59mL
CINCHONA BARK10 [hp_X]/59mL
STRYCHNOS NUX-VOMICA SEED10 [hp_X]/59mL
HYDRASTIS CANADENSIS WHOLE10 [hp_X]/59mL
ATROPA BELLADONNA10 [hp_X]/59mL
HISTAMINE DIHYDROCHLORIDE10 [hp_X]/59mL
TEUCRIUM MARUM10 [hp_X]/59mL
DATURA STRAMONIUM10 [hp_X]/59mL
POTASSIUM DICHROMATE10 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F26P2D4757Internal UNII lookup
292E43P4I9Internal UNII lookup
269XH13919Internal UNII lookup
R763EBH88TInternal UNII lookup
WQZ3G9PF0HInternal UNII lookup
3POA0Q644UInternal UNII lookup
10464S0TAAInternal UNII lookup
G6W4F0V8Z3Internal UNII lookup
T4423S18FMInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
37f4ea81-691f-597b-e063-6294a90a84bdAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61152-600-59Snorestop59 mL in 1 BOTTLE, SPRAYSPRAY598

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SnorestopNUX VOMICA, BELLADONNA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, TEUCRIUM MARUM, HISTAMINUM HYDROCHLORICUM, LAUROCERASUS, CINCHONA, STRAMONIUMGreen Pharmaceuticals Inc37f4ea81-691f-597b-e063-6294a90a84bd2025-08-19WarningsExact identifier
ndc (product): 61152-600

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
61152-600-596115206005959 mL in 1 BOTTLE, SPRAY (61152-600-59) 59 ml2025-06-19NoNoCurrent