Jet Lag

Manufacturer: Newton Laboratories, Inc.
Effective date: 2011-03-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:05:24

Label at a glance#

ProductJet Lag

Active ingredientAluminum Oxide, American Ginseng, Silver Nitrate, Arnica Montana, Arsenic Trioxide, Baptisia Tinctoria, Bryonia Alba Root, Lytta Vesicatoria, Chelidonium Majus, Conium Maculatum Flowering Top, Gelsemium Sempervirens Root, Iodine, Potassium Carbonate, Potassium Iodide, Lycopodium Clavatum Spore, Lycopus Virginicus, Sodium Chloride, Strychnos Nux-vomica Seed, Phosphorus, Phytolacca Americana Root, Pulsatilla Vulgaris, Toxicodendron Pubescens Leaf, Saw Palmetto, Thyroid, Unspecified, Echinacea, Unspecified

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

Jet Lag Formulated for symptoms associated with travel such as fatigue, insomnia, headaches and digestive discomfort.

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, dissolve pellets in purified water. Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Alumina 15x, Aralia quinquefolia 15x, Arg. nit. 15x, Arnica 15x, Arsenicum alb. 15x, Baptisia 15x, Bryonia 15x, Cantharis 15x, Chelidonium majus 15x, Conium 15x, Gelsemium 15x, Iodium 15x, Kali carb. 15x, Kali iod. 15x, Lycopodium 15x, Lycopus virginicus 15x, Nat. mur. 15x, Nux vom. 15x, Phosphorus 15x, Phytolacca 15x, Pulsatilla 15x, Rhus toxicodendron 15x, Sabal 15x, Thyroidinum 15x, Echinacea 3x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with travel such as fatigue, insomnia, headaches and digestive discomfort.

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
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
5f30b278-5791-4113-8781-878a9221ef8a	Product name	2	20230125
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
2a70c781-a755-4d76-b20a-a958acfbdcdc	Product name	2	20190619
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
304592ef-4a8a-4c22-8e8c-af73aa3d60e5	Product name	1	20180703
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22	Product name	1	20180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5c	Product name	1	20180619
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
41e9d6cf-3ed7-4c44-a57e-0685058d0896	Product name	1	20170824
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
5e652c92-68fd-426b-b0e7-5fc64e0b9f99	Product name	1	20170309
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c	Product name	1	20150421
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55714-1118-0	2020-01-31	C162847	48780-1	9d75b9cf-f1a0-f424-e053-dadaa90a57ce	Jet Lag
55714-1118-1	2020-01-31	C162847	48780-1	9d75b9cf-f1a0-f424-e053-dadaa90a57ce	Jet Lag
55714-1118-2	2020-01-31	C162847	48780-1	9d75b9cf-f1a0-f424-e053-dadaa90a57ce	Jet Lag

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55714-1118-0	Jet Lag	7.08 g in 1 BOTTLE, GLASS	PELLET	7.08	1
55714-1118-1	Jet Lag	28.35 g in 1 BOTTLE, GLASS	PELLET	28.35	1
55714-1118-2	Jet Lag	56.7 g in 1 BOTTLE, GLASS	PELLET	56.7	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55714-1118	JET LAG (ALUMINA, ARALIA QUINQUEFOLIA, ARG. NIT., ARNICA, ARSENICUM ALB., BAPTISIA, BRYONIA, CANTHARIS, CHELIDONIUM MAJUS, CONIUM, GELSEMIUM, IODIUM, KALI CARB., KALI IOD., LYCOPODIUM, LYCOPUS VIRGINICUS, NAT. MUR., NUX VOM., PHOSPHORUS, PHYTOLACCA, PULSATILLA, RHUS TOXICODENDRON, SABAL, THYROIDINUM, ECHINACEA) PELLET [NEWTON LABORATORIES, INC.]	1	Legacy NDC, 3 package rows	20140128_113401d2-2169-eb86-ee67-6bea8efed9fc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aluminum Oxide	ACTIVE INGREDIENT	LMI26O6933	1
American Ginseng	ACTIVE INGREDIENT	8W75VCV53Q	1
Arnica Montana	ACTIVE INGREDIENT	O80TY208ZW	1
Arsenic Trioxide	ACTIVE INGREDIENT	S7V92P67HO	1
Baptisia Tinctoria	ACTIVE INGREDIENT	5K1UO2888Y	1
Bryonia Alba Root	ACTIVE INGREDIENT	T7J046YI2B	1
Chelidonium Majus	ACTIVE INGREDIENT	7E889U5RNN	1
Conium Maculatum Flowering Top	ACTIVE INGREDIENT	Q28R5GF371	1
Echinacea, Unspecified	ACTIVE INGREDIENT	4N9P6CC1DX	1
Gelsemium Sempervirens Root	ACTIVE INGREDIENT	639KR60Q1Q	1
Iodine	ACTIVE INGREDIENT	9679TC07X4	1
Lycopodium Clavatum Spore	ACTIVE INGREDIENT	C88X29Y479	1
Lycopus Virginicus	ACTIVE INGREDIENT	TWH5125Q6F	1
Lytta Vesicatoria	ACTIVE INGREDIENT	3Q034RO3BT	1
Phosphorus	ACTIVE INGREDIENT	27YLU75U4W	1
Phytolacca Americana Root	ACTIVE INGREDIENT	11E6VI8VEG	1
Potassium Carbonate	ACTIVE INGREDIENT	BQN1B9B9HA	1
Potassium Iodide	ACTIVE INGREDIENT	1C4QK22F9J	1
Pulsatilla Vulgaris	ACTIVE INGREDIENT	I76KB35JEV	1
Saw Palmetto	ACTIVE INGREDIENT	J7WWH9M8QS	1
Silver Nitrate	ACTIVE INGREDIENT	95IT3W8JZE	1
Sodium Chloride	ACTIVE INGREDIENT	451W47IQ8X	1
Strychnos Nux-vomica Seed	ACTIVE INGREDIENT	269XH13919	1
Thyroid, Unspecified	ACTIVE INGREDIENT	0B4FDL9I6P	1
Toxicodendron Pubescens Leaf	ACTIVE INGREDIENT	6IO182RP7A	1
Aluminum Oxide	ACTIVE MOIETY	LMI26O6933	1
American Ginseng	ACTIVE MOIETY	8W75VCV53Q	1
Arnica Montana	ACTIVE MOIETY	O80TY208ZW	1
Arsenic Cation (3+)	ACTIVE MOIETY	C96613F5AV	1
Baptisia Tinctoria	ACTIVE MOIETY	5K1UO2888Y	1
Bryonia Alba Root	ACTIVE MOIETY	T7J046YI2B	1
Carbonate Ion	ACTIVE MOIETY	7UJQ5OPE7D	1
Chelidonium Majus	ACTIVE MOIETY	7E889U5RNN	1
Chloride Ion	ACTIVE MOIETY	Q32ZN48698	1
Conium Maculatum Flowering Top	ACTIVE MOIETY	Q28R5GF371	1
Echinacea, Unspecified	ACTIVE MOIETY	4N9P6CC1DX	1
Gelsemium Sempervirens Root	ACTIVE MOIETY	639KR60Q1Q	1
Iodide Ion	ACTIVE MOIETY	09G4I6V86Q	1
Iodine	ACTIVE MOIETY	9679TC07X4	1
Lycopodium Clavatum Spore	ACTIVE MOIETY	C88X29Y479	1
Lycopus Virginicus	ACTIVE MOIETY	TWH5125Q6F	1
Lytta Vesicatoria	ACTIVE MOIETY	3Q034RO3BT	1
Phosphorus	ACTIVE MOIETY	27YLU75U4W	1
Phytolacca Americana Root	ACTIVE MOIETY	11E6VI8VEG	1
Pulsatilla Vulgaris	ACTIVE MOIETY	I76KB35JEV	1
Saw Palmetto	ACTIVE MOIETY	J7WWH9M8QS	1
Silver Cation	ACTIVE MOIETY	57N7B0K90A	1
Strychnos Nux-vomica Seed	ACTIVE MOIETY	269XH13919	1
Thyroid, Unspecified	ACTIVE MOIETY	0B4FDL9I6P	1
Toxicodendron Pubescens Leaf	ACTIVE MOIETY	6IO182RP7A	1
Sucrose	INACTIVE INGREDIENT	C151H8M554	1

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

Jet Lag
Alumina, Aralia quinquefolia, Arg. nit., Arnica, Arsenicum alb., Baptisia, Bryonia, Cantharis, Chelidonium majus, Conium, Gelsemium, Iodium, Kali carb., Kali iod., Lycopodium, Lycopus virginicus, Nat. mur., Nux vom., Phosphorus, Phytolacca, Pulsatilla, Rhus toxicodendron, Sabal, Thyroidinum, Echinacea
Aluminum Oxide
American Ginseng
Silver Nitrate
Silver Cation
Arnica Montana
Arsenic Trioxide
Arsenic Cation (3+)
Baptisia Tinctoria
Bryonia Alba Root
Lytta Vesicatoria
Chelidonium Majus
Conium Maculatum Flowering Top
Gelsemium Sempervirens Root
Iodine
Potassium Carbonate
Carbonate Ion
Potassium Iodide
Iodide Ion
Lycopodium Clavatum Spore
Lycopus Virginicus
Sodium Chloride
Chloride Ion
Strychnos Nux-vomica Seed
Phosphorus
Phytolacca Americana Root
Pulsatilla Vulgaris
Toxicodendron Pubescens Leaf
Saw Palmetto
Thyroid, Unspecified
Echinacea, Unspecified
Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-1118	55714-1118-1, 55714-1118-2, 55714-1118-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Oxide	LMI26O6933	ACTIB
American Ginseng	8W75VCV53Q	ACTIB
Silver Nitrate	95IT3W8JZE	ACTIB
Arnica Montana	O80TY208ZW	ACTIB
Arsenic Trioxide	S7V92P67HO	ACTIB
Baptisia Tinctoria	5K1UO2888Y	ACTIB
Bryonia Alba Root	T7J046YI2B	ACTIB
Lytta Vesicatoria	3Q034RO3BT	ACTIB
Chelidonium Majus	7E889U5RNN	ACTIB
Conium Maculatum Flowering Top	Q28R5GF371	ACTIB
Gelsemium Sempervirens Root	639KR60Q1Q	ACTIB
Iodine	9679TC07X4	ACTIB
Potassium Carbonate	BQN1B9B9HA	ACTIB
Potassium Iodide	1C4QK22F9J	ACTIM
Lycopodium Clavatum Spore	C88X29Y479	ACTIB
Lycopus Virginicus	TWH5125Q6F	ACTIB
Sodium Chloride	451W47IQ8X	ACTIB
Strychnos Nux-vomica Seed	269XH13919	ACTIB
Phosphorus	27YLU75U4W	ACTIB
Phytolacca Americana Root	11E6VI8VEG	ACTIB
Pulsatilla Vulgaris	I76KB35JEV	ACTIB
Toxicodendron Pubescens Leaf	6IO182RP7A	ACTIB
Saw Palmetto	J7WWH9M8QS	ACTIB
Thyroid, Unspecified	0B4FDL9I6P	ACTIB
Echinacea, Unspecified	4N9P6CC1DX	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	TABLET, FILM COATED / ORAL		145 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	SUPPOSITORY / RECTAL	NA		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, COATED PELLETS / ORAL	59.8 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	CAPSULE, COATED, EXTENDED RELEASE / ORAL		86 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	TABLET, DELAYED RELEASE / ORAL	295.33 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	POWDER / ORAL		27768 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	LOZENGE / TRANSMUCOSAL		1255 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	GRANULE, FOR SOLUTION / ORAL		42596 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	DROPS / ORAL	NA		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	LOZENGE / BUCCAL	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	SUSPENSION / ORAL		48209 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	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 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 / ORAL	NA		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	CAPSULE, DELAYED RELEASE / ORAL		955 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	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS		308 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, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 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	ELIXIR / ORAL		18000 mg	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 / 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	GRANULE, FOR SUSPENSION / ORAL		31885 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	WAFER / ORAL	155.2 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	INJECTION, SOLUTION / INTRAVENOUS	NA		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	LIQUID / ORAL		37500 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	POWDER, FOR SUSPENSION / ORAL		40017 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	CAPSULE / ORAL		3568 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

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
b8a8592d-20d3-a64d-5ffb-b37e9d175059			113401d2-2169-eb86-ee67-6bea8efed9fc	2011-03-01	Warnings	Exact identifier spl id: b8a8592d-20d3-a64d-5ffb-b37e9d175059 spl set id: 113401d2-2169-eb86-ee67-6bea8efed9fc

Reported adverse events (FAERS/openFDA)#

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