Home NDC 71173-3000-1 BUDDATE REGES INTENSIVE TREATMENT
Product NDC 71173-3000
Requested package NDC 71173-3000-1
11-digit product format 711733000
Labeler code 71173
Product ID 71173-3000_44ced40a-d974-eb5b-e063-6394a90a4ce6
Type HUMAN OTC DRUG
Nonproprietary name Butylene Glycol, Hydrogenated Coconut Oil, Butyrospermum Parkii (Shea) Butter, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7
Dosage form CREAM
Route TOPICAL
Labeler BUDDATE Co Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2017-01-01
Substance BUTYLENE GLYCOL; HYDROGENATED COCONUT OIL; PALMITOYL TETRAPEPTIDE-7; PALMITOYL TRIPEPTIDE-1; SHEA BUTTER
Active strength 5.57; 4; .000006; .000006; 3 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 71173-3000 71173-3000-1 I Inactivated by FDA excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 71173-3000 71173-3000-1 I Inactivated by FDA excluded / ndc_excluded.zip 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 71173-3000 71173-3000-1 I Inactivated by FDA excluded / ndc_excluded.zip a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 71173-3000 71173-3000-1 I Inactivated by FDA excluded / ndc_excluded.zip cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 71173-3000 71173-3000-1 I Inactivated by FDA excluded / ndc_excluded.zip cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 71173-3000 71173-3000-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 71173-3000 71173-3000-1 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 71173-3000 71173-3000-1 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base BUDDATE REGES INTENSIVE TREATMENT
Listing expiration 2026-12-31
Active Ingredients# Ingredient, Strength table Ingredient Strength PALMITOYL TETRAPEPTIDE-7 5.57 g/100mL SHEA BUTTER 4 g/100mL PALMITOYL TRIPEPTIDE-1 .000006 g/100mL BUTYLENE GLYCOL .000006 g/100mL HYDROGENATED COCONUT OIL 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
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 71173-3000-1 BUDDATE REGES INTENSIVE TREATMENT 70 mL in 1 TUBE CREAM 70 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71173-3000 BUDDATE REGES INTENSIVE TREATMENT (BUTYLENE GLYCOL, HYDROGENATED COCONUT OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, PALMITOYL TRIPEPTIDE-1, PALMITOYL TETRAPEPTIDE-7) CREAM [BUDDATE CO LTD] 2 Current NDC, Legacy NDC, 1 package rows 20190220_46495321-fb14-3479-e054-00144ff88e88.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 71173-3000-1 71173300001 70 mL in 1 TUBE (71173-3000-1) 70 ml 2017-01-01 0000-00-00 No No Current