Home NDC 81995-056 First honey Burn Salve
Product NDC 81995-056
11-digit product format 819950056
Labeler code 81995
Product ID 81995-056_2d5e186d-35d6-81b9-e063-6294a90a9daa
Type HUMAN OTC DRUG
Nonproprietary name ALLANTOIN
Dosage form CREAM
Route TOPICAL
Labeler First Honey, LLC
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-05-10
Substance ALLANTOIN
Active strength 5 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 81995-056-02 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 81995-056-01 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 81995-056-02 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 81995-056-01 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81995-056-02 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81995-056-01 0efc9e666f02…f202fb6c5f17…
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 First honey Burn Salve
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 241509 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81995-056-01 First honey Burn Salve 1 in 1 CARTON CREAM 1 4 81995-056-01 First honey Burn Salve 100 mL in 1 TUBE CREAM 100 4 81995-056-02 First honey Burn Salve 1 in 1 CARTON CREAM 1 4 81995-056-02 First honey Burn Salve 5 mL in 1 POUCH CREAM 5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81995-056 FIRST HONEY BURN SALVE (ALLANTOIN) CREAM [FIRST HONEY, LLC] 4 Current NDC, 4 package rows 20250206_f40a9a34-1827-7171-e053-2a95a90acf31.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 39 of 68 · 1,357 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81995-056-01 81995005601 1 TUBE in 1 CARTON (81995-056-01) / 100 mL in 1 TUBE 1 tube 2022-05-10 No No Current 81995-056-02 81995005602 1 POUCH in 1 CARTON (81995-056-02) / 5 mL in 1 POUCH 1 pouch 2023-06-01 No No Current