Ease Remedy Water

Manufacturer: Georgetown Health, LLC DBA EssentiaLife | Newton Laboratories, Inc.
Effective date: 2012-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:04:13

Label at a glance#

ProductEase Remedy Water

Active ingredientAconitum Napellus, Antimony Potassium Tartrate, Silver Nitrate, Arnica Montana, Bryonia Alba Root, Matricaria Recutita, Chelidonium Majus, Black Cohosh, Eupatorium Perfoliatum Flowering Top, Hypericum Perforatum, Strychnos Nux-vomica Seed, Toxicodendron Pubescens Leaf, Ruta Graveolens Flowering Top, Lactic Acid, L-, Datura Stramonium, Strychnine, Phytolacca Americana Root, Comfrey Root

Label structure9 sections

Indications and uses

Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Dosage and administration

Ages 12 and up. Remedy Water ® homepathic pellets are dispersed via the PowerCap ® apparatus. Firmly press PowerCap ® dome to release pellets into the bottle of water and shake well. Remedy Water ® pellets may not dissolve completely. Drink within four hours. Avoid storing or washing where temperatures may exceed 140 degrees.

Storage and handling

Avoid storing in areas where temperatures may exceed 140 degrees.

Contacts and useful links#

PhoneLabel contact1.866.777.1277

Websitewww.remedywater.com

www.RemedyWater.com

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aconitum napellus	15x
Antimonoium tartaricum	15x
Argentum nitricum	15x
Arnica montana	15x
Bryonia	15x
Chamomilla	15x
Chelidonium majus	15x
Cimicifuga racemosa	15x
Eupatorium perfoliatum	15x
Hypericum perforatum	15x
Nux vomica	15x
Rhus toxicodendron	15x
Ruta gravealens	15x
Sarcolacticum acidum	15x
Stramonium	15x
Strychninum	15x
Chamomilla	3x
Phytolacca decandra	3x
Ruta graveolens	3x
Symphytum officinale	3x

Purpose

OTC - PURPOSE SECTION

Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Uses

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Warnings

WARNINGS SECTION

Do not use if tamper-evident package seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Ages 12 and up. Remedy Water^® homepathic pellets are dispersed via the PowerCap^® apparatus. Firmly press PowerCap^® dome to release pellets into the bottle of water and shake well. Remedy Water^® pellets may not dissolve completely. Drink within four hours. Avoid storing or washing where temperatures may exceed 140 degrees.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

USP/NF neutral pellets (.07% gluten-free, non-GMO, beet-derived sucrose, .03% gluten-free, non-GMO maize starch in 500 ml water)

Other Information

STORAGE AND HANDLING SECTION

Avoid storing in areas where temperatures may exceed 140 degrees.

Questions?

OTC - QUESTIONS SECTION

1.866.777.1277
www.RemedyWater.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 35378-0010-2

EssentiaLIFE Homeopathics™

EASE Remedy Water^®

Formulated for symptoms associated with muscle discomfort such as bruising, pain, soreness, stiffness, spasms and weakness.

Seven PowerCaps^® - 1 gram each

Directions: Ages 12 and up. Remedy Water^® homepathic pellets are dispersed via the PowerCap^® apparatus. Firmly press PowerCap^® dome to release pellets into the bottle of water and shake well. Remedy Water^® pellets may not dissolve completely. Drink within four hours. Avoid storing or washing where temperatures may exceed 140 degrees.

IT'S ALL IN THE CAP
NEVER A PRESERVATIVE
1. PUSH
2. SHAKE

Please Recyle

Patent Pending

Boosted by PowerCap^®

FDA Registered and Regulated

NO PRESERVATIVES

ZERO CALORIES

BPA-FREE BOTTLE

Active Ingredients: Aconitum napellus 15x, Antimonium tartaricum 15x, Argentum nitricum 15x, Arnica montana 15x, Bryonia 15x, Chamomilla 15x, Chelidonium majus 15x, Cimicifuga racemosa 15x, Eupatorium perfoliatum 15x, Hypericum perforatum 15x, Nux vomica 15x, Rhus toxicodendron 15x, Ruta graveolens 15x, Sarcolacticum acidum 15x, Stramonium 15x, Strychnium 15x, Chamomilla 3x, Phytolacca decandra 3x, Ruta graveolens 3x, Symphytum officinale 3x.

Inactive ingredients: USP/NF neutral pellets (.07% gluten-free, non-GMO, beet-derived sucrose, .03% gluten-free, non-GMO maize starch in 500 ml water)

Stock# EW05

Lot# 01GEW05

www.RemedyWater.com

Distributed by EssentiaLIFE

FDA Est# 3006407415 Atlanta, GA 30328

Questions?

1.866.777.1277

Warning: Do not use if tamper-evident package seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
35378-0010-2	2020-01-31	C162847	48780-1	9d75b9d0-ebae-f424-e053-dadaa90a57ce	Ease Remedy Water ®
35378-0010-3	2020-01-31	C162847	48780-1	9d75b9d0-ebae-f424-e053-dadaa90a57ce	Ease Remedy Water ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
35378-0010-2	Ease Remedy Water	1000 mg in 1 CYLINDER	PELLET	1000	3
35378-0010-2	Ease Remedy Water	7 in 1 CONTAINER	PELLET	7	3
35378-0010-3	Ease Remedy Water	1 in 1 CONTAINER	PELLET	1	3
35378-0010-3	Ease Remedy Water	1000 mg in 1 CYLINDER	PELLET	1000	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
35378-0010	EASE REMEDY WATER (ACONITUM NAP., ANTIMON. TART., ARG. NIT., ARNICA, BRYONA, CHAMOMILLA, CHELIDONIUM MAJUS, CIMICIFUGA, EUPATORIUM PERF., HYPERICUM, NUX VOM., RHUS TOXICODENDRON, RUTA, SARCOLACTICUM AC., STRAMONIUM, STRYCHNIUM, CHAMOMILLA, PHYTOLACCA, RUTA, SYMPHYTUM) PELLET [GEORGETOWN HEALTH, LLC DBA ESSENTIALIFE]	3	Legacy NDC, 4 package rows	20121220_862d0d52-7a63-196f-daca-53919a3c6de5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aconitum Napellus	ACTIVE INGREDIENT	U0NQ8555JD	3
Antimony Potassium Tartrate	ACTIVE INGREDIENT	DL6OZ476V3	3
Arnica Montana	ACTIVE INGREDIENT	O80TY208ZW	3
Black Cohosh	ACTIVE INGREDIENT	K73E24S6X9	3
Bryonia Alba Root	ACTIVE INGREDIENT	T7J046YI2B	3
Chelidonium Majus	ACTIVE INGREDIENT	7E889U5RNN	3
Comfrey Root	ACTIVE INGREDIENT	M9VVZ08EKQ	3
Datura Stramonium	ACTIVE INGREDIENT	G6W4F0V8Z3	3
Eupatorium Perfoliatum Flowering Top	ACTIVE INGREDIENT	1W0775VX6E	3
Hypericum Perforatum	ACTIVE INGREDIENT	XK4IUX8MNB	3
Lactic Acid, L-	ACTIVE INGREDIENT	F9S9FFU82N	3
Matricaria Recutita	ACTIVE INGREDIENT	G0R4UBI2ZZ	3
Phytolacca Americana Root	ACTIVE INGREDIENT	11E6VI8VEG	3
Ruta Graveolens Flowering Top	ACTIVE INGREDIENT	N94C2U587S	3
Silver Nitrate	ACTIVE INGREDIENT	95IT3W8JZE	3
Strychnine	ACTIVE INGREDIENT	H9Y79VD43J	3
Strychnos Nux-vomica Seed	ACTIVE INGREDIENT	269XH13919	3
Toxicodendron Pubescens Leaf	ACTIVE INGREDIENT	6IO182RP7A	3
Aconitum Napellus	ACTIVE MOIETY	U0NQ8555JD	3
Antimony Cation (3)	ACTIVE MOIETY	069647RPT5	3
Arnica Montana	ACTIVE MOIETY	O80TY208ZW	3
Black Cohosh	ACTIVE MOIETY	K73E24S6X9	3
Bryonia Alba Root	ACTIVE MOIETY	T7J046YI2B	3
Chelidonium Majus	ACTIVE MOIETY	7E889U5RNN	3
Comfrey Root	ACTIVE MOIETY	M9VVZ08EKQ	3
Datura Stramonium	ACTIVE MOIETY	G6W4F0V8Z3	3
Eupatorium Perfoliatum Flowering Top	ACTIVE MOIETY	1W0775VX6E	3
Hypericum Perforatum	ACTIVE MOIETY	XK4IUX8MNB	3
Lactic Acid, L-	ACTIVE MOIETY	F9S9FFU82N	3
Matricaria Recutita	ACTIVE MOIETY	G0R4UBI2ZZ	3
Phytolacca Americana Root	ACTIVE MOIETY	11E6VI8VEG	3
Ruta Graveolens Flowering Top	ACTIVE MOIETY	N94C2U587S	3
Silver Cation	ACTIVE MOIETY	57N7B0K90A	3
Strychnine	ACTIVE MOIETY	H9Y79VD43J	3
Strychnos Nux-vomica Seed	ACTIVE MOIETY	269XH13919	3
Toxicodendron Pubescens Leaf	ACTIVE MOIETY	6IO182RP7A	3
Starch, Corn	INACTIVE INGREDIENT	O8232NY3SJ	3
Sucrose	INACTIVE INGREDIENT	C151H8M554	3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

Ease Remedy Water
Aconitum nap., Antimon. tart., Arg. nit., Arnica, Bryona, Chamomilla, Chelidonium majus, Cimicifuga, Eupatorium perf., Hypericum, Nux vom., Rhus toxicodendron, Ruta, Sarcolacticum ac., Stramonium, Strychnium, Chamomilla, Phytolacca, Ruta, Symphytum
Aconitum Napellus
Antimony Potassium Tartrate
Antimony Cation (3)
Silver Nitrate
Silver Cation
Arnica Montana
Bryonia Alba Root
Matricaria Recutita
Chelidonium Majus
Black Cohosh
Eupatorium Perfoliatum Flowering Top
Hypericum Perforatum
Strychnos Nux-vomica Seed
Toxicodendron Pubescens Leaf
Ruta Graveolens Flowering Top
Lactic Acid, L-
Datura Stramonium
Strychnine
Phytolacca Americana Root
Comfrey Root
Starch, Corn
Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
35378-0010	35378-0010-2, 35378-0010-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aconitum Napellus	U0NQ8555JD	ACTIB
Antimony Potassium Tartrate	DL6OZ476V3	ACTIB
Silver Nitrate	95IT3W8JZE	ACTIB
Arnica Montana	O80TY208ZW	ACTIB
Bryonia Alba Root	T7J046YI2B	ACTIB
Matricaria Recutita	G0R4UBI2ZZ	ACTIB
Chelidonium Majus	7E889U5RNN	ACTIB
Black Cohosh	K73E24S6X9	ACTIB
Eupatorium Perfoliatum Flowering Top	1W0775VX6E	ACTIB
Hypericum Perforatum	XK4IUX8MNB	ACTIB
Strychnos Nux-vomica Seed	269XH13919	ACTIB
Toxicodendron Pubescens Leaf	6IO182RP7A	ACTIB
Ruta Graveolens Flowering Top	N94C2U587S	ACTIB
Lactic Acid, L-	F9S9FFU82N	ACTIB
Datura Stramonium	G6W4F0V8Z3	ACTIB
Strychnine	H9Y79VD43J	ACTIB
Matricaria Recutita	G0R4UBI2ZZ	ACTIB
Phytolacca Americana Root	11E6VI8VEG	ACTIB
Ruta Graveolens Flowering Top	N94C2U587S	ACTIB
Comfrey Root	M9VVZ08EKQ	ACTIB
Starch, Corn	O8232NY3SJ	IACT
Sucrose	C151H8M554	IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 70 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		21 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	SUSPENSION / ORAL		900 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	SUSPENSION, EXTENDED RELEASE / ORAL		113 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CONCENTRATE / ORAL		4800 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	CONCENTRATE / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SOLUTION / INTRAVENOUS	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		2000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, EXTENDED RELEASE / ORAL		619 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, DELAYED RELEASE / ORAL		713 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	POWDER, FOR SUSPENSION / ORAL		34 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	CAPSULE / ORAL		5785 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	CAPSULE, COATED, EXTENDED RELEASE / ORAL		19 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LIQUID / ORAL		37500 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, EMULSION / INTRAVENOUS		970 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	SUSPENSION/ DROPS / ORAL		90 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, FILM COATED / ORAL		2000 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION/ DROPS / ORAL		3750 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER / ORAL		27768 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / ORAL		4249 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUPPOSITORY / RECTAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / ORAL		70000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	CAPSULE, EXTENDED RELEASE / ORAL		194 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, DELAYED RELEASE / ORAL	295.33 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / TRANSMUCOSAL		1255 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	PASTILLE / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, ORALLY DISINTEGRATING / ORAL		100 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE / ORAL		3568 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / RECTAL	35.42 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET / ORAL		1116 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, FILM COATED / ORAL		145 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	WAFER / ORAL	155.2 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	INSERT / VAGINAL		147 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	PASTILLE / ORAL	426 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SUSPENSION / ORAL		40017 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	ELIXIR / ORAL		18000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, CHEWABLE / ORAL		180 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS		308 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / SUBCUTANEOUS	47.75 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / INTRAVENOUS		1950 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	DROPS / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET, EXTENDED RELEASE / ORAL		184 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	TABLET / SUBLINGUAL		409 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	900 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	DROPS / ORAL	NA		Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, CHEWABLE / ORAL		7258 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION / ORAL		31885 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SYRUP / ORAL		46400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SOLUTION / ORAL		38666 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Starch, Corn	STARCH, CORN	O8232NY3SJ	CAPSULE, DELAYED RELEASE / ORAL		216 mg	Exact identifier — unii candidate 22 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION / ORAL		48209 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / BUCCAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, COATED, EXTENDED RELEASE / ORAL		86 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SOLUTION / ORAL		42596 mg	Exact identifier — unii candidate 48 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7cee29cf-2094-93b8-4113-2bc3fccf739b			862d0d52-7a63-196f-daca-53919a3c6de5	2012-06-10	Warnings	Exact identifier spl id: 7cee29cf-2094-93b8-4113-2bc3fccf739b spl set id: 862d0d52-7a63-196f-daca-53919a3c6de5

Reported adverse events (FAERS/openFDA)#

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