Home FDA labels b696bf3c-025a-495a-80ed-e9effdd42efd DIARRHEA CP openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name DIARRHEA CP
Generic name AETHUSA CYNAPIUM, ARSENIC TRIOXIDE, OYSTER SHELL CALICUM CARBONATE, CRUDE, MATRICARIA CHAMOMILLA, CITRULLUS COLOCYNTHIS FRUIT PULP, IRON, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLOBILIS, PHOSPHORUS, PODOPHYLLUM, ANEMONE PULSATILLA, DELPHINIUM STRAPHISAGRIA SEED, SULFUR
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID 06f51c41-1e76-4201-937a-cbaaf6a477af
SPL ID b696bf3c-025a-495a-80ed-e9effdd42efd
Version 4
Effective date 2025-12-10
Source export date 2026-10-27
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 19:45:34 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name DIARRHEA CP openfda.brand_name generic name AETHUSA CYNAPIUM, ARSENIC TRIOXIDE, OYSTER SHELL CALICUM CARBONATE, CRUDE, MATRICARIA CHAMOMILLA, CITRULLUS COLOCYNTHIS FRUIT PULP, IRON, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLOBILIS, PHOSPHORUS, PODOPHYLLUM, ANEMONE PULSATILLA, DELPHINIUM STRAPHISAGRIA SEED, SULFUR openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0059-1 openfda.package_ndc ndc product 43406-0059 openfda.product_ndc ndc11 package 43406005901 derived:openfda.package_ndc spl id b696bf3c-025a-495a-80ed-e9effdd42efd id spl set id 06f51c41-1e76-4201-937a-cbaaf6a477af set_id unii 27YLU75U4W openfda.unii unii 2S713A4VP3 openfda.unii unii 00543AP1JV openfda.unii unii 324Y4038G2 openfda.unii unii 2E32821G6I openfda.unii unii S7V92P67HO openfda.unii unii M6936L953C openfda.unii unii 70FD1KFU70 openfda.unii unii E1UOL152H7 openfda.unii unii G0R4UBI2ZZ openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 openfda.unii unii 23H32AOH17 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.