FDA.reportPublic FDA data

BELLA CP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2016-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:10

Label at a glance#

ProductBELLA CP
Active ingredientACONITUM NAPELLUS, APIS MELLIFERA, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM SULFATE ANHYDROUS, CAUSTICUM, MATRICARIA RECUTITA, GRAPHITE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, ANEMONE PULSATILLA, SILICON DIOXIDE, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Aconitum Nap 30C, Apis Mel 30C, Belladonna 30C, Calc Carb 30C, Calc Sulph 30C, Causticum 30C, Chamomilla 30C, Graphites 30C, Hepar Sulph Calc 30C, Kali Bic 30C, Lachesis 30C, Lycopodium 30C, Merc Solub 30C, Pulsatilla 30C, Silicea 30C, Sulphur 30C, Thuja Occ 30C.

OTC - PURPOSE SECTION

USES: Temporarily relieves headache & pain due to sinus congestion.**

INDICATIONS & USAGE SECTION

USES: Temporarily relieves headache & pain due to sinus congestion.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: 10 drops orally 3 times daily, or as directed by a health care professional.

WARNINGS SECTION

WARNINGS:

* 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Citric Acid, Glycerin, Natural Cherry Flavor, Potassium Sorbate, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

* The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

** These statements have not been reviewed by the FDA. They are based on traditional homeopathic practice.

                                                                                                                                    LOT:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0638-1

BELLA CP

Aches / Pain**

HOMEOPATHIC

1 fl oz (30 mL) / Alcohol Free

Natural Cherry Flavor

GMP Logo   UPC: 877730004741   NON GMO Logo

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0638-12020-01-31C16284748780-19d75b9d1-2772-f424-e053-dadaa90a57ceBELLA CP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0638-1BELLA CP30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0638BELLA CP (ACONITUM NAPELLUS, APIS MELLIFERA, ATROPA BELLADONNA, OYSTER SHELL CLACIUM CARBONATE CRUDE, CALCIUM SULFATE ANHYDROUS, CAUSTICUM, MATRICARIA RECUTITA, GRAPHITE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, ANEMONE PULSATILLA, SILICON DIOXIDE, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG.) LIQUID [NATURAL CREATIONS, INC.]1Legacy NDC, 1 package rows20160929_62aa1413-67fa-42a1-9da8-c3cfae7690bf.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-063843406-0638-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
CALCIUM SULFATE ANHYDROUSE934B3V59HACTIB
CAUSTICUMDD5FO1WKFUACTIB
MATRICARIA RECUTITAG0R4UBI2ZZACTIB
GRAPHITE4QQN74LH4OACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SULFUR70FD1KFU70ACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
CITRIC ACID ACETATEDSO12WL7AUIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7cf3bdfd-776e-4692-9283-ca37b5b5013962aa1413-67fa-42a1-9da8-c3cfae7690bf2016-09-28WarningsExact identifier
spl id: 7cf3bdfd-776e-4692-9283-ca37b5b50139
spl set id: 62aa1413-67fa-42a1-9da8-c3cfae7690bf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.