Equisetum ex herba 15 Special Order

Product NDC
48951-4034
11-digit product format
489514034
Labeler code
48951
Product ID
48951-4034_6c6c1350-3115-38a0-e053-2991aa0a4143
Type
HUMAN OTC DRUG
Nonproprietary name
Equisetum ex herba 15 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
EQUISETUM ARVENSE TOP
Active strength
15 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4034-1Equisetum ex herba 15 Special Order1 mL in 1 AMPULELIQUID12
48951-4034-1Equisetum ex herba 15 Special Order10 in 1 BOXLIQUID102

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZEQUISETUM EX HERBA 15 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZEQUISETUM EX HERBA 15 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XEQUISETUM EX HERBA 15 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0REQUISETUM EX HERBA 15 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4034EQUISETUM EX HERBA 15 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180518_622c5fa6-297a-48b2-9dd1-3dd9d67f32db.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4034-14895140340110 AMPULE in 1 BOX (48951-4034-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent