Rhumatol

Manufacturer: Hello Life, Inc. | King Bio Inc
Effective date: 2018-12-26
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 02:10:37

Label at a glance#

ProductRhumatol Arthitis Symptom and Muscle Pain Relief

Active ingredientACTAEA SPICATA ROOT, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, CAUSTICUM, BLACK COHOSH, FORMIC ACID, HYPERICUM PERFORATUM, LEDUM PALUSTRE TWIG, MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE, PHYTOLACCA AMERICANA ROOT, PULSATILLA VULGARIS, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SALICYLIC ACID, HORSE CHESTNUT, PHOSPHORUS, LITHIUM CARBONATE, SEPIA OFFICINALIS JUICE, ZINC

Label structure11 sections

Indications and uses

to temporarily relieve symptoms commonly associated with arthritis and muscle pain, such as: • pain • inflammation • stiffness • swelling

Dosage and administration

Dispense Rhumatol directly into mouth, or add recommended dosage into 8-12 oz. of purified (non-chlorinated) water and drink. Safe for ages 2 and up.

Storage and handling

• do not use if tamper seal is broken • store in a cool, dry place • product must not come in contact with metal • do not store next to electrical devices or appliances

Contacts and useful links#

PhoneLabel contact1.800.875.0850

Websitewww.rhumatol.com

www.rhumatol.com

Label contents#

Full prescribing information#

Active Ingredients (per dose)

OTC - ACTIVE INGREDIENT SECTION

Actaea spicata HPUS
Aesculus hippocastanum HPUS
Arnica montana HPUS
Bellis perennis HPUS
Bryonia HPUS
Calcarea carbonica HPUS
Calcarea fluorica HPUS
Causticum HPUS
Cimicifuga racemosa HPUS
Formicum acidum HPUS
Hypericum perforatum HPUS
Ledum paulstre HPUS
Lithium carbonicum HPUS
Magnesia phosphorica HPUS
Phosphorus HPUS
Phytolacca decandra HPUS
Pulsatilla HPUS
Rhododendron chrysanthum HPUS
Rhus toxicodendron HPUS
Ruta graveolens HPUS
Salicylicum acidum HPUS
Sepia HPUS
Zincum metallicum HPUS

Each ingredient contains equal volumes of 10X, 30X and LM1 potencies. The letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
Product indications are based on Homeopathic Materia Medica. Product indicatiosn are based on Homeopathic Materia Medica.

Purpose

OTC - PURPOSE SECTION

Actaea spicata HPUS.........................................Pain
Aesculus hippocastanum HPUS.................Weakness
Arnica montana HPUS................................Soreness
Bellis perennis HPUS............Rheumatism symptoms
Bryonia HPUS.............................................Stiffness
Calcarea carbonica HPUS.............Rheumatoid pains
Calcarea fluorica HPUS................................Burning
Causticum HPUS...................................Tearing pain
Cimicifuga racemosa HPUS…...............Restless limbs
Formicum acidum HPUS...........Nodes around joints
Hypericum perforatum HPUS....................Cramping
Ledum paulstre HPUS..................................Swelling
Lithium carbonicum HPUS....Rheumatism symptoms
Magnesia phosphorica HPUS........................Spasms
Phosphorus HPUS..........Paralysis in fingers and toes
Phytolacca decandra HPUS.........................Stiffness
Pulsatilla HPUS........................................Numbness
Rhododendron chrysanthum HPUS......Pain in joints
Rhus toxicodendron HPUS...............Pain in tendons
Ruta graveolens HPUS.............................Weakness
Salicylicum acidum HPUS............................Swelling
Sepia HPUS...........................Stiffness in extremities
Zincum metallicum HPUS..........................Twitching

Uses

INDICATIONS & USAGE SECTION

to temporarily relieve symptoms commonly associated with arthritis and muscle pain, such as:
•   pain
•   inflammation
•   stiffness
•   swelling

Warnings

WARNINGS SECTION

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

• you are taking any other medications
• you have a medical condition

When using this product,

OTC - WHEN USING SECTION

use only as directed.

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms persist or worsen.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Dispense Rhumatol directly into mouth, or add recommended dosage into 8-12 oz. of purified (non-chlorinated) water and drink. Safe for ages 2 and up.

DOSAGE BY WEIGHT

DOSAGE FORMS & STRENGTHS SECTION

30-50 lbs                   1/2 mL
(13.6-22.6 kg)             twice per day

50+ lbs                      1 mL
(22.6+ kg)                  twice per day

External Use: If needed, apply to affected areas 2 - 6 times daily until symptoms improve.

Other information

STORAGE AND HANDLING SECTION

•    do not use if tamper seal is broken
•    store in a cool, dry place
•    product must not come in contact with metal
•    do not store next to electrical devices or appliances

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, potassium sorbate, purified ionized mineral water.

Questions or comments?

OTC - QUESTIONS SECTION

You can email us at info@hellolife.net or call us toll-free at
1.800.875.0850 Monday through Friday, 9am-5pm ET

DESCRIPTION SECTION

30-day supply
dropper included
Rhumatol is made without alcohol or sugar. No gluten added.

Mftd for: HelloLife, Inc.
4460 44th St. SE, Ste C-600
Grand Rapids, MI 49512
FDA Pharmaceutical Establishment
#1053442, #3009727070
www.rhumatol.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49726-004-02

Rhumatol®

Arthritis Symptom and Muscle Pain Relief

To temporarily relieve symptoms commonly associated with arthritis and muscle pain, such as:
•   pain
•   inflammation
•   stiffness
•   swelling

2 fl oz (59 mL)
Homeopathic (OTC) Medicine

RhumatolCarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6e3c022f-0786-43f1-8857-edff89d5153f	Product name	1	20260309
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
b3053bb1-353b-4a0b-bca5-28fe7228957c	Product name	2	20250124
efd58652-cb8f-4018-91ca-4b0eb2ff729f	Product name	7	20240226
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62	Product name	3	20210309
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
8ce6e144-236f-b7be-f690-f06e0c8c6bd3	Product name	2	20170725
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
f09af6ee-c6dd-d0ce-77ad-93508bcdaced	Product name	4	20161205
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
e7e58cd3-cacb-49df-8d34-1ee335614abb	Product name	1	20150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49726-004-02	2020-01-31	C162847	48780-1	9d75b9d1-23e5-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49726-004-02	RhumatolArthitis Symptom and Muscle Pain Relief	1 in 1 CARTON	LIQUID	1		6
49726-004-02	RhumatolArthitis Symptom and Muscle Pain Relief	59 mL in 1 BOTTLE, DROPPER	LIQUID	59		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49726-004	RHUMATOL ARTHITIS SYMPTOM AND MUSCLE PAIN RELIEF (ACTAEA SPICATA, AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CAUSTICUM, CIMICIFUGA RACEMOSA, FORMICUM ACIDUM, HYPERICUM PERFORATUM, LEDUM PAULSTRE, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, PHOSPHORUS, PHYTOLACCA DECANDRA, PULSATILLA, RHODODENDRON CHRYSANTHUM, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SALICYLICUM ACIDUM, SEPIA, ZINCUM METALLICUM) LIQUID [HELLO LIFE, INC.]	6	Legacy NDC, 2 package rows	20181227_14388c93-bb9f-48f6-a743-f36c6f7e4976.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ACTAEA SPICATA ROOT	ACTIVE INGREDIENT	3FU86L9OS0	5
ARNICA MONTANA	ACTIVE INGREDIENT	O80TY208ZW	5
BELLIS PERENNIS	ACTIVE INGREDIENT	2HU33I03UY	5
BLACK COHOSH	ACTIVE INGREDIENT	K73E24S6X9	5
BRYONIA ALBA ROOT	ACTIVE INGREDIENT	T7J046YI2B	5
CALCIUM FLUORIDE	ACTIVE INGREDIENT	O3B55K4YKI	5
CAUSTICUM	ACTIVE INGREDIENT	DD5FO1WKFU	5
FORMIC ACID	ACTIVE INGREDIENT	0YIW783RG1	5
HORSE CHESTNUT	ACTIVE INGREDIENT	3C18L6RJAZ	5
HYPERICUM PERFORATUM	ACTIVE INGREDIENT	XK4IUX8MNB	5
LEDUM PALUSTRE TWIG	ACTIVE INGREDIENT	877L01IZ0P	5
LITHIUM CARBONATE	ACTIVE INGREDIENT	2BMD2GNA4V	5
MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE	ACTIVE INGREDIENT	453COF7817	5
OYSTER SHELL CALCIUM CARBONATE, CRUDE	ACTIVE INGREDIENT	2E32821G6I	5
PHOSPHORUS	ACTIVE INGREDIENT	27YLU75U4W	5
PHYTOLACCA AMERICANA ROOT	ACTIVE INGREDIENT	11E6VI8VEG	5
PULSATILLA VULGARIS	ACTIVE INGREDIENT	I76KB35JEV	5
RHODODENDRON AUREUM LEAF	ACTIVE INGREDIENT	IV92NQJ73U	5
RUTA GRAVEOLENS FLOWERING TOP	ACTIVE INGREDIENT	N94C2U587S	5
SALICYLIC ACID	ACTIVE INGREDIENT	O414PZ4LPZ	5
SEPIA OFFICINALIS JUICE	ACTIVE INGREDIENT	QDL83WN8C2	5
TOXICODENDRON PUBESCENS LEAF	ACTIVE INGREDIENT	6IO182RP7A	5
ZINC	ACTIVE INGREDIENT	J41CSQ7QDS	5
ACTAEA SPICATA ROOT	ACTIVE MOIETY	3FU86L9OS0	5
ARNICA MONTANA	ACTIVE MOIETY	O80TY208ZW	5
BELLIS PERENNIS	ACTIVE MOIETY	2HU33I03UY	5
BLACK COHOSH	ACTIVE MOIETY	K73E24S6X9	5
BRYONIA ALBA ROOT	ACTIVE MOIETY	T7J046YI2B	5
CAUSTICUM	ACTIVE MOIETY	DD5FO1WKFU	5
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	5
FORMIC ACID	ACTIVE MOIETY	0YIW783RG1	5
HORSE CHESTNUT	ACTIVE MOIETY	3C18L6RJAZ	5
HYPERICUM PERFORATUM	ACTIVE MOIETY	XK4IUX8MNB	5
LEDUM PALUSTRE TWIG	ACTIVE MOIETY	877L01IZ0P	5
LITHIUM CATION	ACTIVE MOIETY	8H8Z5UER66	5
MAGNESIUM CATION	ACTIVE MOIETY	T6V3LHY838	5
OYSTER SHELL CALCIUM CARBONATE, CRUDE	ACTIVE MOIETY	2E32821G6I	5
PHOSPHORUS	ACTIVE MOIETY	27YLU75U4W	5
PHYTOLACCA AMERICANA ROOT	ACTIVE MOIETY	11E6VI8VEG	5
PULSATILLA VULGARIS	ACTIVE MOIETY	I76KB35JEV	5
RHODODENDRON AUREUM LEAF	ACTIVE MOIETY	IV92NQJ73U	5
RUTA GRAVEOLENS FLOWERING TOP	ACTIVE MOIETY	N94C2U587S	5
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	5
SEPIA OFFICINALIS JUICE	ACTIVE MOIETY	QDL83WN8C2	5
TOXICODENDRON PUBESCENS LEAF	ACTIVE MOIETY	6IO182RP7A	5
ZINC	ACTIVE MOIETY	J41CSQ7QDS	5
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	5
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	5

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

Rhumatol Arthitis Symptom and Muscle Pain Relief
ACTAEA SPICATA, AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CAUSTICUM, CIMICIFUGA RACEMOSA, FORMICUM ACIDUM, HYPERICUM PERFORATUM, LEDUM PAULSTRE, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, PHOSPHORUS, PHYTOLACCA DECANDRA, PULSATILLA, RHODODENDRON CHRYSANTHUM, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SALICYLICUM ACIDUM, SEPIA, ZINCUM METALLICUM
WATER
POTASSIUM SORBATE
CITRIC ACID MONOHYDRATE
ACTAEA SPICATA ROOT
ARNICA MONTANA
BELLIS PERENNIS
BRYONIA ALBA ROOT
OYSTER SHELL CALCIUM CARBONATE, CRUDE
CALCIUM FLUORIDE
FLUORIDE ION
CAUSTICUM
BLACK COHOSH
FORMIC ACID
HYPERICUM PERFORATUM
LEDUM PALUSTRE TWIG
MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE
MAGNESIUM CATION
PHYTOLACCA AMERICANA ROOT
PULSATILLA VULGARIS
RHODODENDRON AUREUM LEAF
TOXICODENDRON PUBESCENS LEAF
RUTA GRAVEOLENS FLOWERING TOP
SALICYLIC ACID
HORSE CHESTNUT
PHOSPHORUS
LITHIUM CARBONATE
LITHIUM CATION
SEPIA OFFICINALIS JUICE
ZINC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49726-004	49726-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
ACTAEA SPICATA ROOT	3FU86L9OS0	ACTIB
ARNICA MONTANA	O80TY208ZW	ACTIB
BELLIS PERENNIS	2HU33I03UY	ACTIB
BRYONIA ALBA ROOT	T7J046YI2B	ACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE	2E32821G6I	ACTIB
CALCIUM FLUORIDE	O3B55K4YKI	ACTIB
CAUSTICUM	DD5FO1WKFU	ACTIB
BLACK COHOSH	K73E24S6X9	ACTIB
FORMIC ACID	0YIW783RG1	ACTIB
HYPERICUM PERFORATUM	XK4IUX8MNB	ACTIB
LEDUM PALUSTRE TWIG	877L01IZ0P	ACTIB
MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE	453COF7817	ACTIB
PHYTOLACCA AMERICANA ROOT	11E6VI8VEG	ACTIB
PULSATILLA VULGARIS	I76KB35JEV	ACTIB
RHODODENDRON AUREUM LEAF	IV92NQJ73U	ACTIB
TOXICODENDRON PUBESCENS LEAF	6IO182RP7A	ACTIB
RUTA GRAVEOLENS FLOWERING TOP	N94C2U587S	ACTIB
SALICYLIC ACID	O414PZ4LPZ	ACTIB
HORSE CHESTNUT	3C18L6RJAZ	ACTIB
PHOSPHORUS	27YLU75U4W	ACTIB
LITHIUM CARBONATE	2BMD2GNA4V	ACTIB
SEPIA OFFICINALIS JUICE	QDL83WN8C2	ACTIB
ZINC	J41CSQ7QDS	ACTIB

Source Document#

Source XML

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 · 107 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	DOUCHE / VAGINAL	0.07 %w/w		Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	LOTION / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION/ DROPS / TOPICAL	0.01 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	CREAM / VAGINAL	0.49 %w/w		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, CHEWABLE / ORAL	7 mg		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	LOTION / TOPICAL	0.85 %w/w		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INFILTRATION	0.02 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INTRAMUSCULAR		28 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION/ DROPS / OPHTHALMIC	0.05 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		2 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SPRAY, METERED / NASAL		2 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / IONTOPHORESIS	0.02 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INTRACARDIAC	1.05 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	LIQUID / RESPIRATORY (INHALATION)	0.13 %w/w		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INTRATHECAL	ADJ PH		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / PERIDURAL	NA		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INTRALESIONAL	ADJ PH		Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	OINTMENT / TOPICAL		1 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SPRAY / NASAL		9 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION, SOLUTION / INTRAMUSCULAR		26 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	CAPSULE / ORAL		238 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, EXTENDED RELEASE / ORAL		45 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / NASAL	2.8 mg/1ml		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SYSTEM / TOPICAL	0.2 mg		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	POWDER / ORAL		840 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, FILM COATED / ORAL		42 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SUSPENSION / ORAL		269 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / OPHTHALMIC	0.03 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, EFFERVESCENT / ORAL	460 mg		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	GEL / TOPICAL		1 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	POWDER, FOR SOLUTION / TOPICAL	NA		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	CREAM / TOPICAL		4 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / ORAL		446 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SHAMPOO / TOPICAL		17 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / INTRAVENOUS		10 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / INTRABURSAL	ADJ PH		Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION / EPIDURAL	0.02 %w/v		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS		608 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		385 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	TABLET, ORALLY DISINTEGRATING / ORAL		83 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SYSTEM / IONTOPHORESIS	0.2 mg		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	FILM, EXTENDED RELEASE / TRANSDERMAL	1.38 mg		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SUSPENSION/ DROPS / ORAL		19 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SUSPENSION / OPHTHALMIC	ADJ PH		Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	AEROSOL, FOAM / TOPICAL		8 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	FILM / SUBLINGUAL		10 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION/ DROPS / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / TOPICAL		17 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION, SOLUTION, CONCENTRATE / IRRIGATION		1 mg	Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	INJECTION, SOLUTION / INTRA-ARTICULAR	ADJ PH		Exact identifier — unii candidate 88 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / RECTAL	6.67 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	ELIXIR / ORAL	100 mg/5ml		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SOLUTION / BUCCAL	NA		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	SYRUP / ORAL	722 mg/5ml		Exact identifier — unii candidate 88 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	CAPSULE, EXTENDED RELEASE / ORAL		101 mg	Exact identifier — unii candidate 88 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
7df08284-236b-0914-e053-2991aa0aa0fa			14388c93-bb9f-48f6-a743-f36c6f7e4976	2018-12-26	Warnings	Exact identifier spl id: 7df08284-236b-0914-e053-2991aa0aa0fa spl set id: 14388c93-bb9f-48f6-a743-f36c6f7e4976

Reported adverse events (FAERS/openFDA)#

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