Home NDC 48951-1034 Ananassa Resina
Product NDC 48951-1034
11-digit product format 489511034
Labeler code 48951
Product ID 48951-1034_43056a8c-9d84-4728-e063-6294a90ad09d
Type HUMAN OTC DRUG
Nonproprietary name Ananassa Resina
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance PINEAPPLE; SILICON DIOXIDE; LARIX DECIDUA RESIN
Active strength 30; 30; 30 [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fruit Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Ananassa Resina
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PINEAPPLE 30 [hp_X]/1 SILICON DIOXIDE 30 [hp_X]/1 LARIX DECIDUA RESIN 30 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2A88ZO081O Internal UNII lookup ETJ7Z6XBU4 Internal UNII lookup AD8LJ73GQF Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-1034-2 Ananassa Resina 1350 in 1 BOTTLE, GLASS PELLET 1350 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1034 ANANASSA RESINA PELLET [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 1 package rows 20180531_52a18d0a-2c97-4e81-81ff-c836582d0a4c.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-1034-2 48951103402 1350 PELLET in 1 BOTTLE, GLASS (48951-1034-2) 1350 pellet 2009-09-01 0000-00-00 No No Current