Indigestion - Gas

Manufacturer: Newton Laboratories, Inc.
Effective date: 2011-03-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:05:01

Label at a glance#

ProductIndigestion - Gas

Active ingredientBismuth, Aloe, Angelica Sinensis Root, Antimony Trisulfide, Silver Nitrate, Arnica Montana, Arsenic Trioxide, Baptisia Tinctoria, Bryonia Alba Root, Cinchona Officinalis Bark, Graphite, Goldenseal, Ipecac, Lachesis Muta Venom, Lycopodium Clavatum Spore, Myrrh, Sodium Carbonate, Strychnos Nux-vomica Seed, Phosphorus, Pulsatilla Vulgaris, Ginger, Matricaria Recutita, Echinacea, Unspecified, Iris Versicolor Root, Ruta Graveolens Flowering Top, Taraxacum Officinale

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

Indigestion - Gas Formulated for symptoms associated with digestive discomfort such as acid reflux, belching, bloating, bad breath, heartburn, nausea and flatulence.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) as needed or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water. Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Bismuthum metallicum 15x, Aloe 10x, Angelica sinensis radix 10x, Antimon. crud. 10x, Arg. nit. 10x, Arnica 10x, Arsenicum alb. 10x, Baptisia 10x, Bryonia 10x, Cinchona 10x, Graphites 10x, Hydrastis 10x, Ipecac. 10x, Lachesis 10x, Lycopodium 10x, Myrrha 10x, Nat. carb. 10x, Nux vom. 10x, Phosphorus 10x, Pulsatilla 10x, Zingiber 10x, Chamomilla 3x, Echinacea 3x, Iris versicolor 3x, Ruta 3x, Taraxacum 3x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with digestive discomfort such as acid reflux, belching, bloating, bad breath, heartburn, nausea and flatulence.

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: 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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

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
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55714-2239-0	2020-01-31	C162847	48780-1	9d75b9d0-afe7-f424-e053-dadaa90a57ce	Indigestion - Gas
55714-2239-1	2020-01-31	C162847	48780-1	9d75b9d0-afe7-f424-e053-dadaa90a57ce	Indigestion - Gas
55714-2239-2	2020-01-31	C162847	48780-1	9d75b9d0-afe7-f424-e053-dadaa90a57ce	Indigestion - Gas

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55714-2239-0	Indigestion - Gas	7.08 g in 1 BOTTLE, GLASS	PELLET	7.08	2
55714-2239-1	Indigestion - Gas	28.35 g in 1 BOTTLE, GLASS	PELLET	28.35	2
55714-2239-2	Indigestion - Gas	56.7 g in 1 BOTTLE, GLASS	PELLET	56.7	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55714-2239	INDIGESTION - GAS (BISMUTHUM METALLICUM, ALOE, ANGELICA SINENSIS RADIX, ANTIMON. CRUD., ARG. NIT., ARNICA, ARSENICUM ALB., BAPTISIA, BRYONIA, CINCHONA, GRAPHITES, HYDRASTIS, IPECAC., LACHESIS, LYCOPODIUM, MYRRHA, NAT. CARB., NUX VOM., PHOSPHORUS, PULSATILLA, ZINGIBER, CHAMOMILLA, ECHINACEA, IRIS VERSICOLOR, RUTA, TARAXACUM) PELLET [NEWTON LABORATORIES, INC.]	2	Legacy NDC, 3 package rows	20131015_f20b150c-3fa0-5395-da71-d2591ec490ad.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aloe	ACTIVE INGREDIENT	V5VD430YW9	2
Angelica Sinensis Root	ACTIVE INGREDIENT	B66F4574UG	2
Antimony Trisulfide	ACTIVE INGREDIENT	F79059A38U	2
Arnica Montana	ACTIVE INGREDIENT	O80TY208ZW	2
Arsenic Trioxide	ACTIVE INGREDIENT	S7V92P67HO	2
Baptisia Tinctoria	ACTIVE INGREDIENT	5K1UO2888Y	2
Bismuth	ACTIVE INGREDIENT	U015TT5I8H	2
Bryonia Alba Root	ACTIVE INGREDIENT	T7J046YI2B	2
Cinchona Officinalis Bark	ACTIVE INGREDIENT	S003A158SB	2
Echinacea, Unspecified	ACTIVE INGREDIENT	4N9P6CC1DX	2
Ginger	ACTIVE INGREDIENT	C5529G5JPQ	2
Goldenseal	ACTIVE INGREDIENT	ZW3Z11D0JV	2
Graphite	ACTIVE INGREDIENT	4QQN74LH4O	2
Ipecac	ACTIVE INGREDIENT	62I3C8233L	2
Iris Versicolor Root	ACTIVE INGREDIENT	X43D4L3DQC	2
Lachesis Muta Venom	ACTIVE INGREDIENT	VSW71SS07I	2
Lycopodium Clavatum Spore	ACTIVE INGREDIENT	C88X29Y479	2
Matricaria Recutita	ACTIVE INGREDIENT	G0R4UBI2ZZ	2
Myrrh	ACTIVE INGREDIENT	JC71GJ1F3L	2
Phosphorus	ACTIVE INGREDIENT	27YLU75U4W	2
Pulsatilla Vulgaris	ACTIVE INGREDIENT	I76KB35JEV	2
Ruta Graveolens Flowering Top	ACTIVE INGREDIENT	N94C2U587S	2
Silver Nitrate	ACTIVE INGREDIENT	95IT3W8JZE	2
Sodium Carbonate	ACTIVE INGREDIENT	45P3261C7T	2
Strychnos Nux-vomica Seed	ACTIVE INGREDIENT	269XH13919	2
Taraxacum Officinale	ACTIVE INGREDIENT	39981FM375	2
Aloe	ACTIVE MOIETY	V5VD430YW9	2
Angelica Sinensis Root	ACTIVE MOIETY	B66F4574UG	2
Antimony Trisulfide	ACTIVE MOIETY	F79059A38U	2
Arnica Montana	ACTIVE MOIETY	O80TY208ZW	2
Arsenic Cation (3+)	ACTIVE MOIETY	C96613F5AV	2
Baptisia Tinctoria	ACTIVE MOIETY	5K1UO2888Y	2
Bismuth	ACTIVE MOIETY	U015TT5I8H	2
Bryonia Alba Root	ACTIVE MOIETY	T7J046YI2B	2
Carbonate Ion	ACTIVE MOIETY	7UJQ5OPE7D	2
Cinchona Officinalis Bark	ACTIVE MOIETY	S003A158SB	2
Echinacea, Unspecified	ACTIVE MOIETY	4N9P6CC1DX	2
Ginger	ACTIVE MOIETY	C5529G5JPQ	2
Goldenseal	ACTIVE MOIETY	ZW3Z11D0JV	2
Graphite	ACTIVE MOIETY	4QQN74LH4O	2
Ipecac	ACTIVE MOIETY	62I3C8233L	2
Iris Versicolor Root	ACTIVE MOIETY	X43D4L3DQC	2
Lachesis Muta Venom	ACTIVE MOIETY	VSW71SS07I	2
Lycopodium Clavatum Spore	ACTIVE MOIETY	C88X29Y479	2
Matricaria Recutita	ACTIVE MOIETY	G0R4UBI2ZZ	2
Myrrh	ACTIVE MOIETY	JC71GJ1F3L	2
Phosphorus	ACTIVE MOIETY	27YLU75U4W	2
Pulsatilla Vulgaris	ACTIVE MOIETY	I76KB35JEV	2
Ruta Graveolens Flowering Top	ACTIVE MOIETY	N94C2U587S	2
Silver Cation	ACTIVE MOIETY	57N7B0K90A	2
Strychnos Nux-vomica Seed	ACTIVE MOIETY	269XH13919	2
Taraxacum Officinale	ACTIVE MOIETY	39981FM375	2
Sucrose	INACTIVE INGREDIENT	C151H8M554	2

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

Indigestion - Gas
Bismuthum metallicum, Aloe, Angelica sinensis radix, Antimon. crud., Arg. nit., Arnica, Arsenicum alb., Baptisia, Bryonia, Cinchona, Graphites, Hydrastis, Ipecac., Lachesis, Lycopodium, Myrrha, Nat. carb., Nux vom., Phosphorus, Pulsatilla, Zingiber, Chamomilla, Echinacea, Iris versicolor, Ruta, Taraxacum
Bismuth
Aloe
Angelica Sinensis Root
Antimony Trisulfide
Silver Nitrate
Silver Cation
Arnica Montana
Arsenic Trioxide
Arsenic Cation (3+)
Baptisia Tinctoria
Bryonia Alba Root
Cinchona Officinalis Bark
Graphite
Goldenseal
Ipecac
Lachesis Muta Venom
Lycopodium Clavatum Spore
Myrrh
Sodium Carbonate
Carbonate Ion
Strychnos Nux-vomica Seed
Phosphorus
Pulsatilla Vulgaris
Ginger
Matricaria Recutita
Echinacea, Unspecified
Iris Versicolor Root
Ruta Graveolens Flowering Top
Taraxacum Officinale
Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-2239	55714-2239-1, 55714-2239-2, 55714-2239-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Bismuth	U015TT5I8H	ACTIB
Aloe	V5VD430YW9	ACTIB
Angelica Sinensis Root	B66F4574UG	ACTIB
Antimony Trisulfide	F79059A38U	ACTIB
Silver Nitrate	95IT3W8JZE	ACTIB
Arnica Montana	O80TY208ZW	ACTIB
Arsenic Trioxide	S7V92P67HO	ACTIB
Baptisia Tinctoria	5K1UO2888Y	ACTIB
Bryonia Alba Root	T7J046YI2B	ACTIB
Cinchona Officinalis Bark	S003A158SB	ACTIB
Graphite	4QQN74LH4O	ACTIB
Goldenseal	ZW3Z11D0JV	ACTIB
Ipecac	62I3C8233L	ACTIB
Lachesis Muta Venom	VSW71SS07I	ACTIB
Lycopodium Clavatum Spore	C88X29Y479	ACTIB
Myrrh	JC71GJ1F3L	ACTIB
Sodium Carbonate	45P3261C7T	ACTIB
Strychnos Nux-vomica Seed	269XH13919	ACTIB
Phosphorus	27YLU75U4W	ACTIB
Pulsatilla Vulgaris	I76KB35JEV	ACTIB
Ginger	C5529G5JPQ	ACTIB
Matricaria Recutita	G0R4UBI2ZZ	ACTIB
Echinacea, Unspecified	4N9P6CC1DX	ACTIB
Iris Versicolor Root	X43D4L3DQC	ACTIB
Ruta Graveolens Flowering Top	N94C2U587S	ACTIB
Taraxacum Officinale	39981FM375	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	GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL		18790 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	LOZENGE / BUCCAL	NA		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	SUSPENSION / ORAL		48209 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	SOLUTION / RECTAL	35.42 %w/v		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	POWDER, FOR SOLUTION / ORAL		38666 mg	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	INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS	9.4 %w/v		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	CONCENTRATE / ORAL		4800 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	INJECTION / SUBCUTANEOUS	47.75 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	SYRUP / ORAL		46400 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	INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 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	INJECTION, SOLUTION / INTRAVENOUS	NA		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 / SUBLINGUAL	109 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	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	900 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	GRANULE, FOR SOLUTION / ORAL		42596 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	POWDER / ORAL		27768 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
Sucrose	SUCROSE	C151H8M554	ELIXIR / ORAL		18000 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	TABLET, FILM COATED / ORAL		145 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	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 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	LOZENGE / TRANSMUCOSAL		1255 mg	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	SUPPOSITORY / RECTAL	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, DELAYED RELEASE / ORAL	295.33 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, EXTENDED RELEASE / ORAL	284.54 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	SUSPENSION/ DROPS / ORAL		3750 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	TABLET / ORAL		4249 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

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
c97b712e-1ed9-761c-9ce7-73186d4d2f6b			f20b150c-3fa0-5395-da71-d2591ec490ad	2011-03-01	Warnings	Exact identifier spl id: c97b712e-1ed9-761c-9ce7-73186d4d2f6b spl set id: f20b150c-3fa0-5395-da71-d2591ec490ad

Reported adverse events (FAERS/openFDA)#

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