Chrysosplenium Chamomilla

Product NDC
48951-3088
11-digit product format
489513088
Labeler code
48951
Product ID
48951-3088_4bd3ab6e-a571-75f6-e063-6394a90a9f3a
Type
HUMAN OTC DRUG
Nonproprietary name
Chrysosplenium Chamomilla
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
MATRICARIA RECUTITA; CHRYSOSPLENETIN; CICHORIUM INTYBUS WHOLE; TARAXACUM PALUSTRE ROOT
Active strength
3; 3; 6; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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
Chrysosplenium Chamomilla
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MATRICARIA RECUTITA3 [hp_X]/mL
CHRYSOSPLENETIN3 [hp_X]/mL
CICHORIUM INTYBUS WHOLE6 [hp_X]/mL
TARAXACUM PALUSTRE ROOT6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
G0R4UBI2ZZInternal UNII lookup
9AA5Z8PMYEInternal UNII lookup
1KE45XD28SInternal UNII lookup
GCZ4W7077CInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d2c9746c-784b-4d76-874b-4f8ea6814f99Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3088-1Chrysosplenium Chamomilla10 in 1 BOXLIQUID104
48951-3088-1Chrysosplenium Chamomilla1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHRYSOSPLENETINACTIVE INGREDIENT9AA5Z8PMYECHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
CICHORIUM INTYBUS WHOLEACTIVE INGREDIENT1KE45XD28SCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
MATRICARIA RECUTITAACTIVE INGREDIENTG0R4UBI2ZZCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
TARAXACUM PALUSTRE ROOTACTIVE INGREDIENTGCZ4W7077CCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
CHRYSOSPLENETINACTIVE MOIETY9AA5Z8PMYECHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
CICHORIUM INTYBUS WHOLEACTIVE MOIETY1KE45XD28SCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
MATRICARIA RECUTITAACTIVE MOIETYG0R4UBI2ZZCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
TARAXACUM PALUSTRE ROOTACTIVE MOIETYGCZ4W7077CCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3088CHRYSOSPLENIUM CHAMOMILLA LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20180516_d2c9746c-784b-4d76-874b-4f8ea6814f99.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
Chrysosplenium ChamomillaCHRYSOSPLENIUM CHAMOMILLAUriel Pharmacy Inc.d2c9746c-784b-4d76-874b-4f8ea6814f992026-02-27WarningsExact identifier
ndc (product): 48951-3088

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3088-14895130880110 AMPULE in 1 BOX (48951-3088-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent