Natural Response

Manufacturer: Newton Laboratories, Inc.
Effective date: 2014-11-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:06:13

Label at a glance#

ProductNatural Response

Active ingredientAconitum Napellus, Arnica Montana, Arsenic Trioxide, Bryonia Alba Root, Echinacea, Unspecified, Ledum Palustre Twig, Agkistrodon Contortrix Venom, Crotalus Durissus Terrificus Venom, Crotalus Horridus Horridus Venom, Lachesis Muta Venom, Mercuric Chloride, Naja Naja Venom, Phosphorus, Agkistrodon Piscivorus Venom, Vipera Berus Venom, Micrurus Corallinus Venom, Heloderma Suspectum Venom

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1.800.448.7256

Websitewww.newtonlabs.net

www.newtonlabs.net

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with injuries, bites and infections such as restlessness, bleeding, pain, nausea, vomiting, swelling, trembling and confusion.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets by mouth (ages 0 to 11, give 3 pellets) as needed or as directed by a health professional. Under age 2, crush/dissolve pellets in purified water. Sensitive persons begin with 1 pellet and gradually increase to full dose. Warning: For use as an interim therapy. Seek professional medical intervention for severe injuries, bites or infections.

OTC - ACTIVE INGREDIENT SECTION

Aconitum nap. 10x, Arnica 10x, Arsenicum alb. 10x, Bryonia 10x, Echinacea 10x, Ledum 10x, Cenchris 15x, Crotalus casc. 15x, Crotalus hor. 15x, Lachesis 15x, Merc. corros. 15x, Naja 15x, Phos. 15x, Toxicophis 15x, Vipera 15x, Elaps cor. 30x, Heloderma 30x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with injuries, bites and infections such as restlessness, bleeding, pain, nausea, vomiting, swelling, trembling and confusion.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions? 1.800.448.7256

WARNINGS SECTION

Warning: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55714-2367-1	2020-01-31	C162847	48780-1	9d75b9d0-3a72-f424-e053-dadaa90a57ce	Natural Response
55714-2367-2	2020-01-31	C162847	48780-1	9d75b9d0-3a72-f424-e053-dadaa90a57ce	Natural Response

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55714-2367-1	Natural Response	28 g in 1 BOTTLE, GLASS	PELLET	28		1
55714-2367-2	Natural Response	57 g in 1 BOTTLE, GLASS	PELLET	57		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55714-2367	NATURAL RESPONSE (ACONITUM NAP., ARNICA, ARSENICUM ALB., BRYONIA, ECHINACEA, LEDUM, CENCHRIS, CROTALUS CASC. CROTALUS HOR., LACHESIS, MERC. CORROS., NAJA, PHOS., TOXICOPHIS, VIPERA, ELAPS COR., HELODERMA) PELLET [NEWTON LABORATORIES, INC.]	1	Legacy NDC, 2 package rows	20141204_83a604ab-950f-40ec-9e44-fbfa36b04a99.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aconitum Napellus	ACTIVE INGREDIENT	U0NQ8555JD	1
Agkistrodon Contortrix Venom	ACTIVE INGREDIENT	3BKX485ZP0	1
Agkistrodon Piscivorus Venom	ACTIVE INGREDIENT	X9V1Q8U150	1
Arnica Montana	ACTIVE INGREDIENT	O80TY208ZW	1
Arsenic Trioxide	ACTIVE INGREDIENT	S7V92P67HO	1
Bryonia Alba Root	ACTIVE INGREDIENT	T7J046YI2B	1
Crotalus Durissus Terrificus Venom	ACTIVE INGREDIENT	2XF6I0446G	1
Crotalus Horridus Horridus Venom	ACTIVE INGREDIENT	YHA2XLJ956	1
Echinacea, Unspecified	ACTIVE INGREDIENT	4N9P6CC1DX	1
Heloderma Suspectum Venom	ACTIVE INGREDIENT	KV57S96367	1
Lachesis Muta Venom	ACTIVE INGREDIENT	VSW71SS07I	1
Ledum Palustre Twig	ACTIVE INGREDIENT	877L01IZ0P	1
Mercuric Chloride	ACTIVE INGREDIENT	53GH7MZT1R	1
Micrurus Corallinus Venom	ACTIVE INGREDIENT	V0S6H36980	1
Naja Naja Venom	ACTIVE INGREDIENT	ZZ4AG7L7VM	1
Phosphorus	ACTIVE INGREDIENT	27YLU75U4W	1
Vipera Berus Venom	ACTIVE INGREDIENT	0ORO6NCA4M	1
Aconitum Napellus	ACTIVE MOIETY	U0NQ8555JD	1
Agkistrodon Contortrix Venom	ACTIVE MOIETY	3BKX485ZP0	1
Agkistrodon Piscivorus Venom	ACTIVE MOIETY	X9V1Q8U150	1
Arnica Montana	ACTIVE MOIETY	O80TY208ZW	1
Arsenic Cation (3+)	ACTIVE MOIETY	C96613F5AV	1
Bryonia Alba Root	ACTIVE MOIETY	T7J046YI2B	1
Crotalus Durissus Terrificus Venom	ACTIVE MOIETY	2XF6I0446G	1
Crotalus Horridus Horridus Venom	ACTIVE MOIETY	YHA2XLJ956	1
Echinacea, Unspecified	ACTIVE MOIETY	4N9P6CC1DX	1
Heloderma Suspectum Venom	ACTIVE MOIETY	KV57S96367	1
Lachesis Muta Venom	ACTIVE MOIETY	VSW71SS07I	1
Ledum Palustre Twig	ACTIVE MOIETY	877L01IZ0P	1
Mercuric Cation	ACTIVE MOIETY	ED30FJ8Y42	1
Micrurus Corallinus Venom	ACTIVE MOIETY	V0S6H36980	1
Naja Naja Venom	ACTIVE MOIETY	ZZ4AG7L7VM	1
Phosphorus	ACTIVE MOIETY	27YLU75U4W	1
Vipera Berus Venom	ACTIVE MOIETY	0ORO6NCA4M	1
Sucrose	INACTIVE INGREDIENT	C151H8M554	1

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

Natural Response
Aconitum nap., Arnica, Arsenicum alb., Bryonia, Echinacea, Ledum, Cenchris, Crotalus casc. Crotalus hor., Lachesis, Merc. corros., Naja, Phos., Toxicophis, Vipera, Elaps cor., Heloderma
Aconitum Napellus
Arnica Montana
Arsenic Trioxide
Arsenic Cation (3+)
Bryonia Alba Root
Echinacea, Unspecified
Ledum Palustre Twig
Agkistrodon Contortrix Venom
Crotalus Durissus Terrificus Venom
Crotalus Horridus Horridus Venom
Lachesis Muta Venom
Mercuric Chloride
Mercuric Cation
Naja Naja Venom
Phosphorus
Agkistrodon Piscivorus Venom
Vipera Berus Venom
Micrurus Corallinus Venom
Heloderma Suspectum Venom
Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-2367	55714-2367-1, 55714-2367-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aconitum Napellus	U0NQ8555JD	ACTIB
Arnica Montana	O80TY208ZW	ACTIB
Arsenic Trioxide	S7V92P67HO	ACTIM
Bryonia Alba Root	T7J046YI2B	ACTIB
Echinacea, Unspecified	4N9P6CC1DX	ACTIB
Ledum Palustre Twig	877L01IZ0P	ACTIB
Agkistrodon Contortrix Venom	3BKX485ZP0	ACTIB
Crotalus Durissus Terrificus Venom	2XF6I0446G	ACTIB
Crotalus Horridus Horridus Venom	YHA2XLJ956	ACTIB
Lachesis Muta Venom	VSW71SS07I	ACTIB
Mercuric Chloride	53GH7MZT1R	ACTIB
Naja Naja Venom	ZZ4AG7L7VM	ACTIB
Phosphorus	27YLU75U4W	ACTIB
Agkistrodon Piscivorus Venom	X9V1Q8U150	ACTIB
Vipera Berus Venom	0ORO6NCA4M	ACTIB
Micrurus Corallinus Venom	V0S6H36980	ACTIB
Heloderma Suspectum Venom	KV57S96367	ACTIB
Sucrose	C151H8M554	IACT

Source Document#

Source XML

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 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Sucrose	SUCROSE	C151H8M554	INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION/ DROPS / ORAL		3750 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / INTRAVENOUS		1950 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS		308 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / ORAL		4249 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION, EXTENDED RELEASE / ORAL		5400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, DELAYED RELEASE / ORAL		955 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER / ORAL		27768 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SOLUTION / ORAL		42596 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS	9.4 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION / ORAL		48209 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, FILM COATED / ORAL		145 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	900 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUPPOSITORY / RECTAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		2000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SOLUTION / INTRAVENOUS	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, EXTENDED RELEASE / ORAL		619 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, EXTENDED RELEASE / ORAL	284.54 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SOLUTION / ORAL		38666 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	119.12 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	ELIXIR / ORAL		18000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, DELAYED RELEASE / ORAL	295.33 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL		18790 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / SUBCUTANEOUS	47.75 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, COATED, EXTENDED RELEASE / ORAL		86 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / ORAL		70000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	WAFER / ORAL	155.2 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	DROPS / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, CHEWABLE / ORAL		7258 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, COATED / ORAL	516.42 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE / ORAL		3568 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION / ORAL		31885 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	PASTILLE / ORAL	426 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SUSPENSION / ORAL		40017 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / TRANSMUCOSAL		1255 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, COATED PELLETS / ORAL	59.8 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / BUCCAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LIQUID / ORAL		37500 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CONCENTRATE / ORAL		4800 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / RECTAL	35.42 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SYRUP / ORAL		46400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, EMULSION / INTRAVENOUS		970 mg	Exact identifier — unii candidate 48 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
bcb97377-de7d-6300-5e43-da545227e306			83a604ab-950f-40ec-9e44-fbfa36b04a99	2014-11-10	Warnings	Exact identifier spl id: bcb97377-de7d-6300-5e43-da545227e306 spl set id: 83a604ab-950f-40ec-9e44-fbfa36b04a99

Reported adverse events (FAERS/openFDA)#

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