Home DailyMed 93736f0b-a419-4b90-84b0-f27e4c71299b Weight Management HP Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Natural Creations, Inc. | OHM Pharma, Inc.
Effective date 2022-12-20
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-06-01 02:19:28 Label at a glance# Product Weight Management HP
Active ingredient ARSENIC TRIOXIDE, GOLD, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IODINE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, PULSATILLA VULGARIS
Label structure 9 sections
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43406-0053-1 Weight Management HP 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43406-0053 WEIGHT MANAGEMENT HP (ARSENIC TRIOXIDE, GOLD, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IODINE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SULFUR) LIQUID [NATURAL CREATIONS, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20230111_93736f0b-a419-4b90-84b0-f27e4c71299b.zip
DailyMed Socrata Ingredients# Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 17 matching rows.
Weight Management HP Arsenic Trioxide, Gold, Oyster Shell Calcium Carbonate, Crude, Iodine, Lycopodium Clavatum Spore, Sodium Chloride, Strychnos Nux-Vomica Seed, Phosphoric Acid, Phosphorus, Phytolacca Americana Root, Pulsatilla Vulgaris, Sepia Officinalis Juice, Sulfur ARSENIC TRIOXIDE ARSENIC CATION (3+) GOLD OYSTER SHELL CALCIUM CARBONATE, CRUDE IODINE LYCOPODIUM CLAVATUM SPORE SODIUM CHLORIDE CHLORIDE ION STRYCHNOS NUX-VOMICA SEED PHOSPHORIC ACID PHOSPHORUS PHYTOLACCA AMERICANA ROOT PULSATILLA VULGARIS WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 13 matching rows.
Inactive ingredient matches# Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
Inactive ingredient links page 1 of 1 · 2 matching rows.
DailyMed ingredient, IID ingredient, UNII table DailyMed ingredient IID ingredient UNII Dosage form / route Potency Maximum daily exposure Match ALCOHOL ALCOHOL 3K9958V90M LIQUID / ORAL 3563 mg Exact identifier — unii+route+dosage form 2 equally ranked IID candidates ALCOHOL ALCOHOL 3K9958V90M LIQUID / ORAL 3563 mg Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Weight Management HP ARSENIC TRIOXIDE, GOLD, OYSTER SHELL CALCIUM CARBONATE, CRUDE, IODINE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SULFUR Natural Creations, Inc. 93736f0b-a419-4b90-84b0-f27e4c71299b 2022-12-20 Warnings Exact identifier ndc (package): 43406-0053-1 ndc (product): 43406-0053 ndc11 (package): 43406005301 spl id: 5affda02-cfef-481d-934d-45549c0afe1e spl set id: 93736f0b-a419-4b90-84b0-f27e4c71299b
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.