FDA.reportPublic FDA data

Ananassa Resina

Product NDC
48951-1331
11-digit product format
489511331
Labeler code
48951
Product ID
48951-1331_96b174e1-405a-9932-e053-2995a90ac5f3
Type
HUMAN OTC DRUG
Nonproprietary name
Ananassa Resina
Dosage form
CREAM
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
PINEAPPLE; LARIX DECIDUA RESIN; SILICON DIOXIDE
Active strength
2 [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-1331IInactivated by FDA2026-08-10
excluded packagepackage48951-133148951-1331-5IInactivated by FDA2026-08-10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1331-5Ananassa Resina1 in 1 BAGCREAM14
48951-1331-5Ananassa Resina10 g in 1 TUBECREAM104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1331ANANASSA RESINA CREAM [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20240514_96b1507d-d071-1b49-e053-2995a90ad840.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1331-5489511331051 TUBE in 1 BAG (48951-1331-5) > 10 g in 1 TUBE1 tube2009-09-010000-00-00NoNoCurrent