Injury - Rescue
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2011-06-01
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:04:56
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Injury - Rescue Formulated for symptoms associated with injury, trauma or surgery such as pain, shock, emotional upset, bruising and inflammation.
DOSAGE & ADMINISTRATION SECTION
Directions: ORAL USE ONLY - SHAKE WELL. Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) as needed or as directed by a healthcare professional.
ACTIVE INGREDIENT SECTION
Aconitum nap. 20x, Arnica 20x, Bellis 20x, Calendula 20x, Echinacea 20x, Gelsemium 20x, Hamamelis 20x, Hypericum 20x, Ledum 20x, Phosphorus 20x, Rhus toxicodendron 20x, Ruta 20x, Staphysag. 20x, Symphytum 20x, Echinacea 8x, Hydrastis 8x, Hypericum 8x, Symphytum 8x, Echinacea 3x, Hydrastis 3x, Hypericum 3x, Symphytum 3x.
PURPOSE SECTION
Formulated for symptoms associated with injury, trauma or surgery such as pain, shock, emotional upset, bruising and inflammation.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.
QUESTIONS? SECTION
www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions? 1.800.448.7256
WARNINGS SECTION
Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.
PREGNANCY OR BREAST FEEDING SECTION
Consult a licensed healthcare professional if pregnant or nursing or if symptoms worsen or persist for more than a few days.
KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
PACKAGE LABEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55714-4504-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-12f4-f424-e053-dadaa90a57ce | Injury - Rescue |
| 55714-4504-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-12f4-f424-e053-dadaa90a57ce | Injury - Rescue |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55714-4504-1 | Injury - Rescue | 29.57 mL in 1 BOTTLE, GLASS | LIQUID | 29.57 | 2 | |
| 55714-4504-2 | Injury - Rescue | 59.14 mL in 1 BOTTLE, GLASS | LIQUID | 59.14 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55714-4504 | INJURY - RESCUE (ACONITUM NAP., ARNICA, BELLIS , CALENDULA , ECHINACEA, GELSEMIUM, HAMAMELIS, HYPERICUM , LEDUM, PHOSPHORUS, RHUS TOXICODENDRON, RUTA, STAPHYSAG., SYMPHYTUM, HYDRASTIS) LIQUID [NEWTON LABORATORIES, INC.] | 2 | Legacy NDC, 2 package rows | 20130829_8568bf08-4d78-9c52-89ed-3772fec1dfee.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Aconitum Napellus | ACTIVE INGREDIENT | U0NQ8555JD | 2 | |
| Arnica Montana | ACTIVE INGREDIENT | O80TY208ZW | 2 | |
| Bellis Perennis | ACTIVE INGREDIENT | 2HU33I03UY | 2 | |
| Calendula Officinalis Flowering Top | ACTIVE INGREDIENT | 18E7415PXQ | 2 | |
| Comfrey Root | ACTIVE INGREDIENT | M9VVZ08EKQ | 2 | |
| Delphinium Staphisagria Seed | ACTIVE INGREDIENT | 00543AP1JV | 2 | |
| Echinacea, Unspecified | ACTIVE INGREDIENT | 4N9P6CC1DX | 2 | |
| Gelsemium Sempervirens Root | ACTIVE INGREDIENT | 639KR60Q1Q | 2 | |
| Goldenseal | ACTIVE INGREDIENT | ZW3Z11D0JV | 2 | |
| Hamamelis Virginiana Root Bark/stem Bark | ACTIVE INGREDIENT | T7S323PKJS | 2 | |
| Hypericum Perforatum | ACTIVE INGREDIENT | XK4IUX8MNB | 2 | |
| Ledum Palustre Twig | ACTIVE INGREDIENT | 877L01IZ0P | 2 | |
| Phosphorus | ACTIVE INGREDIENT | 27YLU75U4W | 2 | |
| Ruta Graveolens Flowering Top | ACTIVE INGREDIENT | N94C2U587S | 2 | |
| Toxicodendron Pubescens Leaf | ACTIVE INGREDIENT | 6IO182RP7A | 2 | |
| Aconitum Napellus | ACTIVE MOIETY | U0NQ8555JD | 2 | |
| Arnica Montana | ACTIVE MOIETY | O80TY208ZW | 2 | |
| Bellis Perennis | ACTIVE MOIETY | 2HU33I03UY | 2 | |
| Calendula Officinalis Flowering Top | ACTIVE MOIETY | 18E7415PXQ | 2 | |
| Comfrey Root | ACTIVE MOIETY | M9VVZ08EKQ | 2 | |
| Delphinium Staphisagria Seed | ACTIVE MOIETY | 00543AP1JV | 2 | |
| Echinacea, Unspecified | ACTIVE MOIETY | 4N9P6CC1DX | 2 | |
| Gelsemium Sempervirens Root | ACTIVE MOIETY | 639KR60Q1Q | 2 | |
| Goldenseal | ACTIVE MOIETY | ZW3Z11D0JV | 2 | |
| Hamamelis Virginiana Root Bark/stem Bark | ACTIVE MOIETY | T7S323PKJS | 2 | |
| Hypericum Perforatum | ACTIVE MOIETY | XK4IUX8MNB | 2 | |
| Ledum Palustre Twig | ACTIVE MOIETY | 877L01IZ0P | 2 | |
| Phosphorus | ACTIVE MOIETY | 27YLU75U4W | 2 | |
| Ruta Graveolens Flowering Top | ACTIVE MOIETY | N94C2U587S | 2 | |
| Toxicodendron Pubescens Leaf | ACTIVE MOIETY | 6IO182RP7A | 2 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 2 |
Products#
Every source-derived product name is available through these pages.
- Injury - Rescue
- Aconitum nap., Arnica, Bellis , Calendula , Echinacea, Gelsemium, Hamamelis, Hypericum , Ledum, Phosphorus, Rhus toxicodendron, Ruta, Staphysag., Symphytum, Hydrastis
- Aconitum Napellus
- Arnica Montana
- Bellis Perennis
- Calendula Officinalis Flowering Top
- Echinacea, Unspecified
- Gelsemium Sempervirens Root
- Hamamelis Virginiana Root Bark/stem Bark
- Hypericum Perforatum
- Ledum Palustre Twig
- Phosphorus
- Toxicodendron Pubescens Leaf
- Ruta Graveolens Flowering Top
- Delphinium Staphisagria Seed
- Comfrey Root
- Goldenseal
- Alcohol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-4504 | 55714-4504-1, 55714-4504-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 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 |
|---|---|---|---|---|---|---|
| 4b612dec-6226-8bbc-bb57-c902bf2d69e7 | 8568bf08-4d78-9c52-89ed-3772fec1dfee | 2011-06-01 | Warnings | 4b612dec-6226-8bbc-bb57-c902bf2d69e7 8568bf08-4d78-9c52-89ed-3772fec1dfee |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
