Cichorium Oxalis

Product NDC
48951-3091
11-digit product format
489513091
Labeler code
48951
Product ID
48951-3091_4bada4cc-42b1-239c-e063-6394a90a52cb
Type
HUMAN OTC DRUG
Nonproprietary name
Cichorium Oxalis
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ACTIVATED CHARCOAL; BARIUM CITRATE; CICHORIUM INTYBUS WHOLE; IRON; OXALIS ACETOSELLA LEAF; SUS SCROFA PANCREAS
Active strength
6; 10; 3; 20; 3; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cichorium Oxalis
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACTIVATED CHARCOAL6 [hp_X]/mL
BARIUM CITRATE10 [hp_X]/mL
CICHORIUM INTYBUS WHOLE3 [hp_X]/mL
IRON20 [hp_X]/mL
OXALIS ACETOSELLA LEAF3 [hp_X]/mL
SUS SCROFA PANCREAS6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2P3VWU3H10, J9X0Y34WC2, 1KE45XD28S, E1UOL152H7, U1W3U02EW0, 9Y3J3362RY

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3091-1Cichorium Oxalis10 in 1 BOXLIQUID104
48951-3091-1Cichorium Oxalis1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H10CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
BARIUM CITRATEACTIVE INGREDIENTJ9X0Y34WC2CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
CICHORIUM INTYBUS WHOLEACTIVE INGREDIENT1KE45XD28SCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
IRONACTIVE INGREDIENTE1UOL152H7CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE INGREDIENTU1W3U02EW0CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE INGREDIENT9Y3J3362RYCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H10CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
ANHYDROUS CITRIC ACIDACTIVE MOIETYXF417D3PSLCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
CICHORIUM INTYBUS WHOLEACTIVE MOIETY1KE45XD28SCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
IRONACTIVE MOIETYE1UOL152H7CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
OXALIS MONTANA LEAFACTIVE MOIETYU1W3U02EW0CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE MOIETY9Y3J3362RYCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3091CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20240203_3d284b66-6a25-4d6f-9d37-e7642ae88d3b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3091-14895130910110 AMPULE in 1 BOX (48951-3091-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent