Formica 3 Special Order

Product NDC
48951-4121
11-digit product format
489514121
Labeler code
48951
Product ID
48951-4121_55a39ec3-beb6-158d-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Formica 3 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
FORMICA RUFA
Active strength
3 [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
48951-4121-1Formica 3 Special Order10 in 1 BOXLIQUID102
48951-4121-1Formica 3 Special Order1 mL in 1 AMPULELIQUID12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FORMICA RUFAACTIVE INGREDIENT55H0W83JO5FORMICA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
FORMICA RUFAACTIVE MOIETY55H0W83JO5FORMICA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XFORMICA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RFORMICA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4121FORMICA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180518_b58dbcd8-6bd7-4b03-828b-45e40b2fb8ab.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4121-14895141210110 AMPULE in 1 BOX (48951-4121-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent