FDA.reportPublic FDA data

ADENOSINE CYCLIC PHOSPHATE

Manufacturer
King Bio Inc.
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:48:57

Label at a glance#

ProductAllergies Desert U.S.
Active ingredientADENOSINE CYCLIC PHOSPHATE, EPINEPHRINE, CORTICOTROPIN, MEDICAGO SATIVA WHOLE, ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ARISAEMA TRIPHYLLUM ROOT, ARUNDO PLINIANA ROOT, CORTISONE ACETATE, ERECHTITES HIERACIIFOLIUS WHOLE, ERIGERON CANADENSIS WHOLE, EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, SODIUM CHLORIDE, SACCHAROMYCES CEREVISIAE RNA, SCHOENOCAULON OFFICINALE SEED, DATURA STRAMONIUM, ELYMUS REPENS ROOT
Label structure9 sections

Indications and uses

For temporary relief of symptoms: red, itchy, watery eyes, sore throat, cough, runny nose, sneezing, congestion, headaches, hoarseness, & fatigue.  Reference image:Allergies Desert.jpg 

Dosage and administration

Initially, depress pump until primed. Spray one dose directly into mouth. Adults: 3 sprays 3 times per day. Children (6 - 12): 2 sprays 3 times per day. Consult a physician for use in children under 6 years of age. Use additionally as needed, up to 6 times per day. Reference image:Allergies Desert.jpg

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

Stop use and ask your doctor if symptoms
persist or worsen.

If pregnant or breast-feeding, take only on
advice of a healthcare professional.

Keep out of reach of children.

Reference image:Allergies Desert.jpg

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Reference image:Allergies Desert.jpg

Directions

DOSAGE & ADMINISTRATION SECTION

Initially, depress pump until
primed. Spray one dose directly into mouth.

Adults: 3 sprays 3 times per day.
Children (6 - 12): 2 sprays 3 times per day.
Consult a physician for use in children
under 6 years of age.

Use additionally as
needed, up to 6 times per day.

Reference image:Allergies Desert.jpg

OTHER SAFETY INFORMATION

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

King Bio, Inc. FDA Reg. #1053442
3 Westside Dr. Asheville, NC 28806 USA
Questions? Call 866.298.2740

Reference image:Allergies Desert.jpg

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Equal volumes of each HPUS ingredient in 12X, 30X,100X, 1LM, 

2LM, 3LM, 5LM potencies, unless otherwise noted. 

Adenosinum
cyclophosphoricum, Adrenalinum,
Adrenocorticotrophin (30X, 100X), Alfalfa, Allium
cepa, Ambrosia, Arum triph, Arundo mauritanica,
Cortisone aceticum, Erechtites, Erigeron,
Euonymus atrop, Euphrasia, Galphimia, Nat mur,
RNA, Sabadilla, Stramonium, Triticum.

Reference image: Allergies Desert.jpg

Uses

INDICATIONS & USAGE SECTION

For temporary relief of symptoms: red,
itchy, watery eyes, sore throat, cough, runny nose,
sneezing, congestion, headaches, hoarseness,
& fatigue. 

Reference image:Allergies Desert.jpg 

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citrus Extract (ascorbic
acid, citric acid, citrus aurantium amara fruit
extract, citrus aurantium sinensis peel extract,
citrus reticulata fruit extract, demineralized water,
glycerin, lactic acid), Honeysuckle (Lonicera
japonica), Polylysine, Purified Water, Shagbark
Hickory (Carya ovata) Bark Extract, Steviol
(Steviol glycosides).

Reference image: Allergies Desert.jpg 

OTC - PURPOSE SECTION

For temporary relief of symptoms:

Red, itchy, watery eyes

Sore throat

Cough

Runny nose

Sneezing

Congestion

Headaches

Hoarseness

Fatigue

Reference image:Allergies Desert.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description Allergies Desert.jpgimage description Allergies Desert.jpg

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-272257955-2722-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
ADENOSINE CYCLIC PHOSPHATEE0399OZS9NACTIB
EPINEPHRINEYKH834O4BHACTIB
CORTICOTROPINK0U68Q2TXAACTIB
MEDICAGO SATIVA WHOLEDJO934BRBDACTIB
ONION492225Q21HACTIB
AMBROSIA ARTEMISIIFOLIA WHOLE9W34L2CQ9AACTIB
ARISAEMA TRIPHYLLUM ROOTDM64K844DMACTIB
ARUNDO PLINIANA ROOTZXE7LB03WCACTIB
CORTISONE ACETATE883WKN7W8XACTIB
ERECHTITES HIERACIIFOLIUS WHOLE1L6JHK0ORRACTIB
ERIGERON CANADENSIS WHOLE16D08B0B9NACTIB
EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARKWJK59V19EWACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
GALPHIMIA GLAUCA FLOWERING TOP93PH5Q8M7EACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
SACCHAROMYCES CEREVISIAE RNAJ17GBZ5VGXACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
DATURA STRAMONIUMG6W4F0V8Z3ACTIB
ELYMUS REPENS ROOT3IXW0F6P8WACTIB
ASCORBIC ACIDPQ6CK8PD0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CITRUS AURANTIUM FRUIT OIL59JDQ5VT0TIACT
ORANGE PEELTI9T76XD44IACT
CITRUS RETICULATA FRUIT OIL25P9H3QU5EIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LACTIC ACID, UNSPECIFIED FORM33X04XA5ATIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
POLYEPSILON-LYSINE (4000 MW)WB0M8X4TWRIACT
CARYA OVATA BARKX765CF609LIACT
STEVIOL4741LYX6RTIACT

Source Document#

Source XML

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
554eaf32-7af8-4d64-856c-b31419aa43fa7cd9d021-67d2-42cc-b113-8ae1d5a416c22025-05-16WarningsExact identifier
spl set id: 7cd9d021-67d2-42cc-b113-8ae1d5a416c2

Reported adverse events (FAERS/openFDA)#

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