ADENOSINE CYCLIC PHOSPHATE

Manufacturer: King Bio Inc.
Effective date: 2018-05-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:10:00

Label at a glance#

ProductAllergies Desert U.S.

Active ingredientADENOSINE CYCLIC PHOSPHATE, EPINEPHRINE, CORTICOTROPIN, ALFALFA, ONION, AMBROSIA ARTEMISIIFOLIA, CORTISONE ACETATE, ERECHTITES HIERACIIFOLIUS, CONYZA CANADENSIS, EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, POTASSIUM CHLORIDE, SUS SCROFA NASAL MUCOSA, SODIUM CHLORIDE, SACCHAROMYCES CEREVISIAE RNA, SCHOENOCAULON OFFICINALE SEED, DATURA STRAMONIUM, ELYMUS REPENS ROOT

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts__________________________________________________________________________________________________________

HPUS active ingredients: Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin (30X, 100X), Alfalfa, Allium cepa, Ambrosia, Cortisone aceticum, Erechtites, Erigeron, Euonymus atrop, Euphrasia, Galphimia, Histaminum hydrochloricum, Kali mur, Mucosa nas, Nat mur, RNA, Sabadilla, Stramonium, Triticum. Equal volumes of each ingredient in 12X, 30X, 100X, 1LM, 2LM, 3LM, 5LM potencies.

INDICATIONS & USAGE SECTION

Uses for temporary relief of symptoms: red, itchy, watery eyes, sore throat, cough, hoarseness, fatigue, runny nose, sneezing, congestion and headache.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, Carya ovata bark extract, citrus extract, Lonicera japonica (honeysuckle), polylysine, steviol glycosides.

WARNINGS SECTION

Warnings

Stop use and ask your doctor if symptoms persist or worsen.
If pregnant or breast-feeding, take only on advice of a healthcare professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Initially, depress pump until primed.
Spray one dose directly into mouth.
Adults 12 and up: 3 sprays 3 times per day.
Children 2-12: 2 sprays 3 times per day.
Children 2 mo-2yr: 1 sprary 3 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if seal is intact. This product has not been clinically tested.

OTC - PURPOSE SECTION

Uses for temporary relief of symptoms:

red, itchy, watery eyes
sore throat
cough
hoarseness
fatigue
runny nose
sneezing
congestion
headache

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
57955-2718-2	2020-01-31	C162847	48780-1	9d75b9d0-d555-f424-e053-dadaa90a57ce	Allergies: Desert U.S.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
57955-2718-2	Allergies Desert U.S.	59 mL in 1 BOTTLE, SPRAY	LIQUID	59		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57955-2718	ALLERGIES DESERT U.S. (ADENOSINUM CYCLOPHOSPHORICUM, ADRENALINUM, ADRENOCORTICOTROPHIN, ALFALFA, ALLIUM CEPA, AMBROSIA, CORTISONE ACETICUM, ERECHTITES, ERIGERON, EUONYMUS ATROP, EUPHRASIA, GALPHIMIA, HISTAMINUM HYDROCHLORICUM, KALI MUR, MUCOSA NAS, NAT MUR, RNA, SABADILLA, STRAMONIUM, TRITICUM.) LIQUID [KING BIO INC.]	2	Legacy NDC, 1 package rows	20180526_4c63ac20-f590-48a4-9754-67223a5a517c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ADENOSINE CYCLIC PHOSPHATE	ACTIVE INGREDIENT	E0399OZS9N	1
ALFALFA	ACTIVE INGREDIENT	DJO934BRBD	1
AMBROSIA ARTEMISIIFOLIA	ACTIVE INGREDIENT	9W34L2CQ9A	1
CONYZA CANADENSIS	ACTIVE INGREDIENT	16D08B0B9N	1
CORTICOTROPIN	ACTIVE INGREDIENT	K0U68Q2TXA	1
CORTISONE ACETATE	ACTIVE INGREDIENT	883WKN7W8X	1
DATURA STRAMONIUM	ACTIVE INGREDIENT	G6W4F0V8Z3	1
ELYMUS REPENS ROOT	ACTIVE INGREDIENT	3IXW0F6P8W	1
EPINEPHRINE	ACTIVE INGREDIENT	YKH834O4BH	1
ERECHTITES HIERACIIFOLIUS	ACTIVE INGREDIENT	1L6JHK0ORR	1
EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK	ACTIVE INGREDIENT	WJK59V19EW	1
EUPHRASIA STRICTA	ACTIVE INGREDIENT	C9642I91WL	1
GALPHIMIA GLAUCA FLOWERING TOP	ACTIVE INGREDIENT	93PH5Q8M7E	1
HISTAMINE DIHYDROCHLORIDE	ACTIVE INGREDIENT	3POA0Q644U	1
ONION	ACTIVE INGREDIENT	492225Q21H	1
POTASSIUM CHLORIDE	ACTIVE INGREDIENT	660YQ98I10	1
SACCHAROMYCES CEREVISIAE RNA	ACTIVE INGREDIENT	J17GBZ5VGX	1
SCHOENOCAULON OFFICINALE SEED	ACTIVE INGREDIENT	6NAF1689IO	1
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	1
SUS SCROFA NASAL MUCOSA	ACTIVE INGREDIENT	ID3Z1X61WY	1
ADENOSINE CYCLIC PHOSPHATE	ACTIVE MOIETY	E0399OZS9N	1
ALFALFA	ACTIVE MOIETY	DJO934BRBD	1
AMBROSIA ARTEMISIIFOLIA	ACTIVE MOIETY	9W34L2CQ9A	1
CHLORIDE ION	ACTIVE MOIETY	Q32ZN48698	1
CONYZA CANADENSIS	ACTIVE MOIETY	16D08B0B9N	1
CORTICOTROPIN	ACTIVE MOIETY	K0U68Q2TXA	1
CORTISONE	ACTIVE MOIETY	V27W9254FZ	1
DATURA STRAMONIUM	ACTIVE MOIETY	G6W4F0V8Z3	1
ELYMUS REPENS ROOT	ACTIVE MOIETY	3IXW0F6P8W	1
EPINEPHRINE	ACTIVE MOIETY	YKH834O4BH	1
ERECHTITES HIERACIIFOLIUS	ACTIVE MOIETY	1L6JHK0ORR	1
EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK	ACTIVE MOIETY	WJK59V19EW	1
EUPHRASIA STRICTA	ACTIVE MOIETY	C9642I91WL	1
GALPHIMIA GLAUCA FLOWERING TOP	ACTIVE MOIETY	93PH5Q8M7E	1
HISTAMINE	ACTIVE MOIETY	820484N8I3	1
ONION	ACTIVE MOIETY	492225Q21H	1
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	1
SACCHAROMYCES CEREVISIAE RNA	ACTIVE MOIETY	J17GBZ5VGX	1
SCHOENOCAULON OFFICINALE SEED	ACTIVE MOIETY	6NAF1689IO	1
SUS SCROFA NASAL MUCOSA	ACTIVE MOIETY	ID3Z1X61WY	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	1
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

Allergies Desert U.S.
Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium cepa, Ambrosia, Cortisone aceticum, Erechtites, Erigeron, Euonymus atrop, Euphrasia, Galphimia, Histaminum hydrochloricum, Kali mur, Mucosa nas, Nat mur, RNA, Sabadilla, Stramonium, Triticum.
ADENOSINE CYCLIC PHOSPHATE
EPINEPHRINE
CORTICOTROPIN
ALFALFA
ONION
AMBROSIA ARTEMISIIFOLIA
CORTISONE ACETATE
CORTISONE
ERECHTITES HIERACIIFOLIUS
CONYZA CANADENSIS
EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK
EUPHRASIA STRICTA
GALPHIMIA GLAUCA FLOWERING TOP
HISTAMINE DIHYDROCHLORIDE
HISTAMINE
POTASSIUM CHLORIDE
POTASSIUM CATION
SUS SCROFA NASAL MUCOSA
SODIUM CHLORIDE
CHLORIDE ION
SACCHAROMYCES CEREVISIAE RNA
SCHOENOCAULON OFFICINALE SEED
DATURA STRAMONIUM
ELYMUS REPENS ROOT
WATER
CARYA OVATA BARK
CITRUS BIOFLAVONOIDS
LONICERA JAPONICA FLOWER
POLYEPSILON-LYSINE (4000 MW)
REBAUDIOSIDE A

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
57955-2718	57955-2718-2

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
ADENOSINE CYCLIC PHOSPHATE	E0399OZS9N	ACTIB
EPINEPHRINE	YKH834O4BH	ACTIB
CORTICOTROPIN	K0U68Q2TXA	ACTIB
ALFALFA	DJO934BRBD	ACTIB
ONION	492225Q21H	ACTIB
AMBROSIA ARTEMISIIFOLIA	9W34L2CQ9A	ACTIB
CORTISONE ACETATE	883WKN7W8X	ACTIB
ERECHTITES HIERACIIFOLIUS	1L6JHK0ORR	ACTIB
CONYZA CANADENSIS	16D08B0B9N	ACTIB
EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK	WJK59V19EW	ACTIB
EUPHRASIA STRICTA	C9642I91WL	ACTIB
GALPHIMIA GLAUCA FLOWERING TOP	93PH5Q8M7E	ACTIB
HISTAMINE DIHYDROCHLORIDE	3POA0Q644U	ACTIB
POTASSIUM CHLORIDE	660YQ98I10	ACTIM
SUS SCROFA NASAL MUCOSA	ID3Z1X61WY	ACTIB
SODIUM CHLORIDE	451W47IQ8X	ACTIB
SACCHAROMYCES CEREVISIAE RNA	J17GBZ5VGX	ACTIB
SCHOENOCAULON OFFICINALE SEED	6NAF1689IO	ACTIB
DATURA STRAMONIUM	G6W4F0V8Z3	ACTIB
ELYMUS REPENS ROOT	3IXW0F6P8W	ACTIB
WATER	059QF0KO0R	IACT
CARYA OVATA BARK	X765CF609L	IACT
CITRUS BIOFLAVONOIDS	BD70459I50	IACT
LONICERA JAPONICA FLOWER	4465L2WS4Y	IACT
POLYEPSILON-LYSINE (4000 MW)	WB0M8X4TWR	IACT
REBAUDIOSIDE A	B3FUD0528F	IACT

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 · 80 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION, SOLUTION, CONCENTRATE / INTRAVENOUS		81 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SOLUTION / TOPICAL	4.35 %w/v		Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, CHEWABLE / ORAL		4 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SUSPENSION/ DROPS / OPHTHALMIC	0.05 %w/v		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		48 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, EFFERVESCENT / ORAL		840 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET / SUBLINGUAL		36 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	CAPSULE, LIQUID FILLED / ORAL		360 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	POWDER, FOR SOLUTION / ORAL		123 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION, SOLUTION / INTRAMUSCULAR		25 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION / INTRAVENOUS		1152 mg	Exact identifier — unii candidate 61 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
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	CONCENTRATE / ORAL		84 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	LOZENGE / TRANSMUCOSAL		44 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	FILM, SOLUBLE / ORAL		7 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	FILM / BUCCAL		9 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	AEROSOL, FOAM / TOPICAL		6 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SOLUTION / RESPIRATORY (INHALATION)		5 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SOLUTION / OPHTHALMIC	0.09 %w/v		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION / INTRACARDIAC		25 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	LIQUID / INTRAVENOUS		18 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	GEL / TOPICAL		3 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SYRUP / ORAL		268 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SOLUTION / ORAL		3900 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET / ORAL		197 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION / INFILTRATION	0.02 %w/v		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION / SUBCUTANEOUS		101 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	CLOTH / TOPICAL	4.2 mg		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SUSPENSION/ DROPS / ORAL		15 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, ORALLY DISINTEGRATING / ORAL		46 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SPRAY / NASAL		5 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	FILM / SUBLINGUAL		11 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	CREAM / TOPICAL		1 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, CHEWABLE, EXTENDED RELEASE / ORAL		12 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, ORALLY DISINTEGRATING / SUBLINGUAL	ADJ PH		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SHAMPOO / TOPICAL	0.07 %w/w		Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / RECTAL	6.67 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET, EXTENDED RELEASE / ORAL		312 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SUSPENSION / RESPIRATORY (INHALATION)		1 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	SPRAY / TOPICAL	0.01 %w/w		Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CREAM / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	AEROSOL / TOPICAL	0.08 %w/w		Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	CAPSULE / ORAL		131 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	LOTION / TOPICAL		211 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	TABLET / BUCCAL		30 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	EMULSION / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	POWDER, FOR SUSPENSION / ORAL		570 mg	Exact identifier — unii candidate 61 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
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	ELIXIR / ORAL		90 mg	Exact identifier — unii candidate 61 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	AEROSOL, FOAM / TOPICAL		8 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	INJECTION / PERINEURAL	0.02 %w/v		Exact identifier — unii candidate 61 equally ranked IID candidates
ANHYDROUS CITRIC ACID	ANHYDROUS CITRIC ACID	XF417D3PSL	PASTE / ORAL		26 mg	Exact identifier — unii candidate 61 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
ca97beea-9303-4fad-bf5e-032641297611			4c63ac20-f590-48a4-9754-67223a5a517c	2018-05-25	Warnings	Exact identifier spl id: ca97beea-9303-4fad-bf5e-032641297611 spl set id: 4c63ac20-f590-48a4-9754-67223a5a517c

Reported adverse events (FAERS/openFDA)#

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