RAD HP
- Manufacturer
- Natural Creations, Inc. | OHM Pharma, Inc.
- Effective date
- 2013-01-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:04:15
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Arsenicum Album 30C, Baptisia Tinctoria 30C, Cadmium Sulphate 30C, Calcarea Fluorica 30C, Cantharis Vesicatoria 30C, Carcinosinum 30C, China Officinalis 30C, Cobalt Metal 30C, Conium Maculatum 30C, Fluoricum Acidum 30C, Hydrastis Canadensis 30C, Iodum Purum 30C, Ipecacuanha 30C, Kreosotum 30C, Phosphorus 30C, Radium Bromatum 30C, Sepia Succus 30C, Silica Terra 30C, Sol 30C, Uranium Nitricum 30C
INDICATIONS & USAGE SECTION
USES: Temporarily relieves restlessness, fevers & chills, aches & pains.
WARNINGS SECTION
WARNING:
Consult a physician for us 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.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.
OTC - DO NOT USE SECTION
OTHER INFORMATION: Tamper Seal: "Sealed for your protection."
Do not use if seal is broken or missing.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alocohol 20%
OTC - QUESTIONS SECTION
QUESTIONS AND COMMENTS?
MFG FOR: Natural Creations / Woodbine, IA / 51579 712.647.1600
LOT:
OTC - PURPOSE SECTION
USES: Temporarily relieves restlessness, fevers & chills, aches & pains.
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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC: 43406-0112-1
RAD HP
Restlessness * Fevers & Chills * Aches
HOMEOPATHIC
1 fl oz (30 mL) / 20% Alcohol
UPC: 877730004208
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
| 5f30b278-5791-4113-8781-878a9221ef8a | Product name | 2 | 20230125 |
| 2a70c781-a755-4d76-b20a-a958acfbdcdc | Product name | 2 | 20190619 |
| 304592ef-4a8a-4c22-8e8c-af73aa3d60e5 | Product name | 1 | 20180703 |
| ac0821a1-ce75-4ea7-880a-59eecaecdf22 | Product name | 1 | 20180703 |
| db5dc4f9-b907-46f6-8fb7-babcf04bbe5c | Product name | 1 | 20180619 |
| 41e9d6cf-3ed7-4c44-a57e-0685058d0896 | Product name | 1 | 20170824 |
| 5e652c92-68fd-426b-b0e7-5fc64e0b9f99 | Product name | 1 | 20170309 |
| ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c | Product name | 1 | 20150421 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43406-0112-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-ddab-cd31-e053-dbdaa90ab51a | RAD HP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43406-0112-1 | RAD HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43406-0112 | RAD HP (ARSENIC TRIOXIDE, BAPTISIA TINCTORIA ROOT, CADMIUM SULFIDE, CALCIUM FLUORIDE, LYTTA VESICATORIA, HUMAN BREAST TUMOR CELL, CINCHONA OFFICINALIS BARK, COBALT, CONIUM MACULATUM FLOWERING TOP, HYDROFLUORIC ACID, GOLDENSEAL, IODINE, IPECAC, WOOD CREOSOTE, PHOSPHORUS, RADIUM BROMIDE, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, URANYL NITRATE HEXAHYDRATE) LIQUID [NATURAL CREATIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20130115_90d1f57c-ae78-4b59-acfc-a5cc49698a2b.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ARSENIC TRIOXIDE | ACTIVE INGREDIENT | S7V92P67HO | 1 | |
| BAPTISIA TINCTORIA ROOT | ACTIVE INGREDIENT | 5EF0HWI5WU | 1 | |
| CADMIUM SULFIDE | ACTIVE INGREDIENT | 057EZR4Z7Q | 1 | |
| CALCIUM FLUORIDE | ACTIVE INGREDIENT | O3B55K4YKI | 1 | |
| CINCHONA OFFICINALIS BARK | ACTIVE INGREDIENT | S003A158SB | 1 | |
| COBALT | ACTIVE INGREDIENT | 3G0H8C9362 | 1 | |
| CONIUM MACULATUM FLOWERING TOP | ACTIVE INGREDIENT | Q28R5GF371 | 1 | |
| GOLDENSEAL | ACTIVE INGREDIENT | ZW3Z11D0JV | 1 | |
| HUMAN BREAST TUMOR CELL | ACTIVE INGREDIENT | C62OO7VD9K | 1 | |
| HYDROFLUORIC ACID | ACTIVE INGREDIENT | RGL5YE86CZ | 1 | |
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | 1 | |
| IPECAC | ACTIVE INGREDIENT | 62I3C8233L | 1 | |
| LYTTA VESICATORIA | ACTIVE INGREDIENT | 3Q034RO3BT | 1 | |
| PHOSPHORUS | ACTIVE INGREDIENT | 27YLU75U4W | 1 | |
| RADIUM BROMIDE | ACTIVE INGREDIENT | R74O7T8569 | 1 | |
| SEPIA OFFICINALIS JUICE | ACTIVE INGREDIENT | QDL83WN8C2 | 1 | |
| SILICON DIOXIDE | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 1 | |
| URANYL NITRATE HEXAHYDRATE | ACTIVE INGREDIENT | 3V057702FY | 1 | |
| WOOD CREOSOTE | ACTIVE INGREDIENT | 3JYG22FD73 | 1 | |
| ARSENIC CATION (3+) | ACTIVE MOIETY | C96613F5AV | 1 | |
| BAPTISIA TINCTORIA ROOT | ACTIVE MOIETY | 5EF0HWI5WU | 1 | |
| CADMIUM CATION | ACTIVE MOIETY | T494FZ4G8G | 1 | |
| CINCHONA OFFICINALIS BARK | ACTIVE MOIETY | S003A158SB | 1 | |
| COBALT | ACTIVE MOIETY | 3G0H8C9362 | 1 | |
| COLLOIDAL SILICON DIOXIDE | ACTIVE MOIETY | ETJ7Z6XBU4 | 1 | |
| CONIUM MACULATUM FLOWERING TOP | ACTIVE MOIETY | Q28R5GF371 | 1 | |
| FLUORIDE ION | ACTIVE MOIETY | Q80VPU408O | 1 | |
| GOLDENSEAL | ACTIVE MOIETY | ZW3Z11D0JV | 1 | |
| HUMAN BREAST TUMOR CELL | ACTIVE MOIETY | C62OO7VD9K | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | 1 | |
| IPECAC | ACTIVE MOIETY | 62I3C8233L | 1 | |
| LYTTA VESICATORIA | ACTIVE MOIETY | 3Q034RO3BT | 1 | |
| PHOSPHORUS | ACTIVE MOIETY | 27YLU75U4W | 1 | |
| RADIUM CATION | ACTIVE MOIETY | 05456MVL7T | 1 | |
| SEPIA OFFICINALIS JUICE | ACTIVE MOIETY | QDL83WN8C2 | 1 | |
| URANIUM CATION (6+) | ACTIVE MOIETY | 5PI36AS4G7 | 1 | |
| WOOD CREOSOTE | ACTIVE MOIETY | 3JYG22FD73 | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- RAD HP
- Arsenic Trioxide, Baptisia Tinctoria Root, Cadmium Sulfide, Calcium Fluoride, Lytta Vesicatoria, Human Breast Tumor Cell, Cinchona Officinalis Bark, Cobalt, Conium Maculatum Flowering Top, Hydrofluoric Acid, Goldenseal, Iodine, Ipecac, Wood Creosote, Phosphorus, Radium Bromide, Sepia Officinalis Juice, Silicon Dioxide, Uranyl Nitrate Hexahydrate
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- BAPTISIA TINCTORIA ROOT
- CADMIUM SULFIDE
- CADMIUM CATION
- CALCIUM FLUORIDE
- FLUORIDE ION
- LYTTA VESICATORIA
- HUMAN BREAST TUMOR CELL
- CINCHONA OFFICINALIS BARK
- COBALT
- CONIUM MACULATUM FLOWERING TOP
- HYDROFLUORIC ACID
- GOLDENSEAL
- IODINE
- IPECAC
- WOOD CREOSOTE
- PHOSPHORUS
- RADIUM BROMIDE
- RADIUM CATION
- SEPIA OFFICINALIS JUICE
- SILICON DIOXIDE
- COLLOIDAL SILICON DIOXIDE
- URANYL NITRATE HEXAHYDRATE
- URANIUM CATION (6+)
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43406-0112 | 43406-0112-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIM |
| BAPTISIA TINCTORIA ROOT | 5EF0HWI5WU | ACTIB |
| CADMIUM SULFIDE | 057EZR4Z7Q | ACTIM |
| CALCIUM FLUORIDE | O3B55K4YKI | ACTIM |
| LYTTA VESICATORIA | 3Q034RO3BT | ACTIB |
| HUMAN BREAST TUMOR CELL | C62OO7VD9K | ACTIB |
| CINCHONA OFFICINALIS BARK | S003A158SB | ACTIB |
| COBALT | 3G0H8C9362 | ACTIB |
| CONIUM MACULATUM FLOWERING TOP | Q28R5GF371 | ACTIB |
| HYDROFLUORIC ACID | RGL5YE86CZ | ACTIM |
| GOLDENSEAL | ZW3Z11D0JV | ACTIB |
| IODINE | 9679TC07X4 | ACTIB |
| IPECAC | 62I3C8233L | ACTIB |
| WOOD CREOSOTE | 3JYG22FD73 | ACTIB |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| RADIUM BROMIDE | R74O7T8569 | ACTIM |
| SEPIA OFFICINALIS JUICE | QDL83WN8C2 | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| URANYL NITRATE HEXAHYDRATE | 3V057702FY | ACTIM |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0d828797-eebd-4727-8d0d-9a17e790f5d0 | 90d1f57c-ae78-4b59-acfc-a5cc49698a2b | 2013-01-02 | Warnings | 0d828797-eebd-4727-8d0d-9a17e790f5d0 90d1f57c-ae78-4b59-acfc-a5cc49698a2b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
