NDC 61571-618 - Nose Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 61571-618
Package NDCs from labels: 61571-618-15
Manufacturer: HomeoPet, LLC | Speciality Pharma Manufacturing LLC | Herbamed
Effective date: 2024-11-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nose Relief - HomeoPet, LLC \| Speciality Pharma Manufacturing LLC \| Herbamed	HomeoPet, LLC \| Speciality Pharma Manufacturing LLC \| Herbamed	2024-11-21	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61571-618-15	Nose Relief	15 mL in 1 BOTTLE, DROPPER	LIQUID	15		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61571-618	NOSE RELIEF (ACONITUM NAP,ALLIUM CEPA,ARG NIT,ARNICA,ARSENICUM ALB,ASAFOETIDA,ASCLEPIAS,AUR MET,BERBER V,CALC CARB,CALC FLUOR,CALC PHOS,CALC SULPH,CHAMOMILLA,CHININUM AR,ECHINACEA,EUPHRASIA,FERRUM PHOS,GELSEMIUM,HEKLA,HEPAR SULPH,HYDRASTIS,KALI BIC,KALI MUR,KALI SULPH,LACHESIS,LYCOPODIUM,MERC SOLUB,MERC SULPH RUB,NAT MUR,NAT SULPH,NIT AC,PHOS,PULSATILLA,PYROGENIUM,RHUS TOX,SABADILLA,SAMBUCUS,SILICEA,SINUSITISINUM,SPIGELIA,SULPHUR,SYMPHYTUM,TEUCRIUM,THUJA) LIQUID [HOMEOPET, LLC]	10	1 package rows	20241124_9bd63335-ddf5-40b3-b76f-e73abae2bae6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CALCIUM SULFIDE	ACTIVE INGREDIENT	1MBW07J51Q	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE INGREDIENT	639KR60Q1Q	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
HYDROCHLORIC ACID	ACTIVE INGREDIENT	QTT17582CB	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
POTASSIUM IODIDE	ACTIVE INGREDIENT	1C4QK22F9J	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
SODIUM ARSENATE, DIBASIC	ACTIVE INGREDIENT	ANU034TUJ4	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
ARSENATE ION	ACTIVE MOIETY	G1DBI405OK	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
CALCIUM SULFIDE	ACTIVE MOIETY	1MBW07J51Q	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE MOIETY	639KR60Q1Q	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
HYDROCHLORIC ACID	ACTIVE MOIETY	QTT17582CB	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
IODIDE ION	ACTIVE MOIETY	09G4I6V86Q	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	NOSE RELIEF (HEPAR SULPHURIS CALCAREM, KALI IODATUM, GELSEMIUM SEMPERVIRENS, NATRUM ARSENICOSUM, MURIATICUM ACIDUM) LIQUID [HOMEOPET, LLC]	3

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 77 of 411 · 8,215 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Anti Bacterial Hand Gel Disney Princess Ariel	ALCOHOL	Bath & Body Works, Inc.	38e2113f-2fce-90f7-e063-6394a90a754c	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti-BacterialHandSpray Sweater Weather	ALCOHOL	Bath & Body Works, Inc.	4629294b-c756-6477-e063-6294a90a3d5d	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Disney Villains Maleficent	ALCOHOL	Bath & Body Works, Inc.	45c39e1e-e48c-a285-e063-6294a90ac2c7	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel In The Stars	ALCOHOL	Bath & Body Works, Inc.	45c4cd42-cdde-4e07-e063-6394a90a2a0f	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Strawberry Snowflakes	ALCOHOL	Bath & Body Works, Inc.	46135c55-58fb-fe01-e063-6394a90ac415	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Pumpkin Pecan Waffles	ALCOHOL	Bath & Body Works, Inc.	45c6b183-8dce-8120-e063-6394a90abdc9	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Sweater Weather	ALCOHOL	Bath & Body Works, Inc.	45c7071a-7a05-7ba1-e063-6294a90af89e	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Vanilla Bean Noel	ALCOHOL	Bath & Body Works, Inc.	45c75b3d-c267-203f-e063-6394a90ae7b4	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Moonlit Goddess	ALCOHOL	Bath & Body Works, Inc.	45c889cd-c377-d8c9-e063-6294a90a74b1	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Winter	ALCOHOL	Bath & Body Works, Inc.	46136f12-b335-98c2-e063-6294a90a00af	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Snowflakes and Cashmere	ALCOHOL	Bath & Body Works, Inc.	4604db79-ddbe-c83d-e063-6394a90aadd8	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Honey Wildflower	ALCOHOL	Bath & Body Works, Inc.	46153052-5e6e-b8d3-e063-6294a90a60fc	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Freshwater	ALCOHOL	Bath & Body Works, Inc.	4613a872-0967-c800-e063-6394a90a22d0	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Pink Bubble Gum	ALCOHOL	Bath & Body Works, Inc.	4614de38-80f8-26db-e063-6294a90ab4f8	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Winterberry Ice	ALCOHOL	Bath & Body Works, Inc.	46138a35-e974-a8bb-e063-6394a90a5b54	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Adrenaline	ALCOHOL	Bath & Body Works, Inc.	4613bfd7-77ff-e237-e063-6394a90ad3d6	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Fiji White Sands	ALCOHOL	Bath & Body Works, Inc.	461420e0-a5b1-81df-e063-6394a90a94ec	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
Anti Bacterial Hand Gel Winter	ALCOHOL	Bath & Body Works, Inc.	4613ce33-6881-e7c8-e063-6394a90a4090	2026-03-09	Warnings	Exact identifier unii: 3K9958V90M
RENAFORCE	BERBERIS VULGARIS, ECHINACEA (ANGUSTIFOLIA), COCCUS CACTI, KALI MURIATICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM	BioActive Nutritional, Inc.	804b7055-e1e6-448d-8257-c562b971f437	2026-03-09	Warnings	Exact identifier unii: 411VRN1TV4 unii: 1TH8Q20J0U unii: VB06AV5US8 unii: 660YQ98I10 unii: C88X29Y479
Vermiclear	GRANATUM, RHAMNUS PURSHIANA, JUGLANS REGIA, FILIX MAS, ABSINTHIUM, AESCULUS HIPPOCASTANUM, ARSENICUM ALBUM, BAPTISIA TINCTORIA, CINA, CINCHONA OFFICINALIS, CUPRUM METALLICUM, IPECACUANHA, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, NUX VOMICA, PODOPHYLLUM PELTATUM, PULSATILLA (VULGARIS), RATANHIA, RHUS TOX, SABADILLA, SILICEA, SPIGELIA ANTHELMIA, TEREBINTHINA, TEUCRIUM MARUM	Energique, Inc.	f7cf3edd-2451-4a4f-b1f2-1b3db2bb4dca	2026-03-09	Warnings	Exact identifier unii: ETJ7Z6XBU4 unii: 6IO182RP7A unii: S7V92P67HO unii: WYT05213GE unii: 6NAF1689IO unii: 10464S0TAA unii: C88X29Y479

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.