Citrus Cydonia 5%

Product NDC
48951-3104
11-digit product format
489513104
Labeler code
48951
Product ID
48951-3104_4886d877-b551-1478-e063-6294a90af471
Type
HUMAN OTC DRUG
Nonproprietary name
CITRUS CYDONIA 5%
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
LEMON; QUINCE
Active strength
1; 1 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Fruit Proteins [EXT], Fruit Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Citrus Cydonia 5%
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LEMON1 [hp_X]/mL
QUINCE1 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
24RS0A988OInternal UNII lookup
12MCS4H09NInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e8eaf4e0-baae-4879-a069-4ffe49faad72Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3104-1Citrus Cydonia 5%10 in 1 BOXLIQUID106
48951-3104-1Citrus Cydonia 5%1 mL in 1 AMPULELIQUID16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LEMONACTIVE INGREDIENT24RS0A988OCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1
QUINCEACTIVE INGREDIENT12MCS4H09NCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1
LEMONACTIVE MOIETY24RS0A988OCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1
QUINCEACTIVE MOIETY12MCS4H09NCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3104CITRUS CYDONIA 5% LIQUID [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 2 package rows20241208_e8eaf4e0-baae-4879-a069-4ffe49faad72.zip

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
Citrus Cydonia 5%CITRUS CYDONIA 5%Uriel Pharmacy Inc.e8eaf4e0-baae-4879-a069-4ffe49faad722026-01-16WarningsExact identifier
ndc (product): 48951-3104

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3104-14895131040110 AMPULE in 1 BOX (48951-3104-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent