United States · FDA National Drug Code directory
BUDDATE REGES INTENSIVE TREATMENT
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71173-3000_44ced40a-d974-eb5b-e063-6394a90a4ce6
- Product NDC
- 71173-3000
- Form
- CREAM
- Composition / generic term
- Butylene Glycol, Hydrogenated Coconut Oil, Butyrospermum Parkii (Shea) Butter, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7
- Labeler
- BUDDATE Co Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20170101
- Source listing expiry
- 20261231
Source-listed ingredients
- PALMITOYL TETRAPEPTIDE-7 — .000006 g/100mL
- SHEA BUTTER — 3 g/100mL
- PALMITOYL TRIPEPTIDE-1 — .000006 g/100mL
- BUTYLENE GLYCOL — 5.57 g/100mL
- HYDROGENATED COCONUT OIL — 4 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 70 mL in 1 TUBE (71173-3000-1) · 71173-3000-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →