Betula Argentum

Product NDC
48951-2063
11-digit product format
489512063
Labeler code
48951
Product ID
48951-2063_3894ea71-3636-1458-e063-6394a90a08fd
Type
HUMAN OTC DRUG
Nonproprietary name
Betula Argentum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
APIS MELLIFERA; ARNICA MONTANA; BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; FORMICA RUFA; SILVER
Active strength
3; 17; 3; 3; 7; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Betula Argentum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
APIS MELLIFERA3 [hp_X]/mL
ARNICA MONTANA17 [hp_X]/mL
BETULA PUBESCENS BARK3 [hp_X]/mL
BETULA PUBESCENS LEAF3 [hp_X]/mL
FORMICA RUFA7 [hp_X]/mL
SILVER8 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7S82P3R43Z, O80TY208ZW, 3R504894L9, 84SOH0O3OO, 55H0W83JO5, 3M4G523W1G

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2063-1Betula Argentum10 in 1 BOXLIQUID104
48951-2063-1Betula Argentum1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43ZBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
BETULA PUBESCENS BARKACTIVE INGREDIENT3R504894L9BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
BETULA PUBESCENS LEAFACTIVE INGREDIENT84SOH0O3OOBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE INGREDIENT55H0W83JO5BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
APIS MELLIFERAACTIVE MOIETY7S82P3R43ZBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
BETULA PUBESCENS BARKACTIVE MOIETY3R504894L9BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
BETULA PUBESCENS LEAFACTIVE MOIETY84SOH0O3OOBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE MOIETY55H0W83JO5BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RBETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2063BETULA ARGENTUM LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20180423_7f436fc5-0983-4ce3-9951-e68e395bcab0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-2063-14895120630110 AMPULE in 1 BOX (48951-2063-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent