SHINGLES PAIN ULCERATION RELIEF

Manufacturer: Liddell Laboratories, Inc. | Apotheca Company
Effective date: 2018-05-10
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-02 00:58:35

Label at a glance#

ProductSHINGLES PAIN ULCERATION RELIEF

Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, CROTON TIGLIUM SEED, SODIUM CHLORIDE, PLANTAGO MAJOR, TOXICODENDRON PUBESCENS LEAF, SMILAX REGELII ROOT

Label structure9 sections

Dosage and administration

Adults and children over 12: Spray liberally on affected area as needed. Children 12 and under: Consult a doctor prior to use.

Contacts and useful links#

PhoneLabel contact1-800-460-7733

Websitewww.liddell.net

WWW.LIDDELL.NET

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

CALENDULA OFFICINALIS 12X, CROTON TIGLIUM 30X, NATRUM MURIATICUM 30X, PLANTAGO MAJOR 30X, RHUS TOX 30X, SARSAPRILLA (SMILAX REGELII) 30X

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve pain due to inflammation caused by but not limited to the following: itching and sensitivity, eruptions, blisters.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For external use only.

If symptoms persist, consult a doctor.

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not get into eyes.

Do not use if TAMPER EVIDENT seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray liberally on affected area as needed. Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve pain due to inflammation caused by but not limited to the following: itching and sensitivity, eruptions, blisters.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF JUICE (ALOE VERA 10X CONCENTRATE), ARNICA MONTANA (FLOWER), LARREA TRIDENTATA (LEAF), SYMPHYTUM OFFICINALE (LEAF), CROTON LECHLERI (SAP), INSTANTIZED SOLUBLE EGGSHELL MEMBRANE + (BIOVADERM BRAND WITH 1% SUNFLOWER LECITHIN), LAVANDULA ANGUSTIFOLIA (BUDS), IONIC COLLOIDAL SILVER, MELISSA OFFICINALIS (LEAF), [PEG-33, PEG-8 DIMETHICONE, PEG-14 (SILSENSE COPOLYOL-1 SILICONE)], [PHENOXYETHANOL, CAPRYLYL GLYCOL, SORBIC ACID (OPTIPHEN-PLUS)], PHYTOLACCA AMERICANA (BERRIES), PHYTOLACCA AMERICANA (ROOT), POTASSIUM SORBATE, PURIFIED WATER, SODIUM BICARBONATE, HYPERICUM PERFORATUM (AERIAL PARTS), TOCOPHEROL [VITAMIN E OIL](DERIVED FROM SOY BEAN), VITAMIN C POWDER (ASCORBIC ACID), WHEY PROTEIN CONCENTRATE, SALIX ALBA (BARK), ACHILLEA MILLEFOLIUM (FLOWER)

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY LIDDELL LABORATORIES, INC. WOODBINE, IA

51579 www.LIDDELL.NET 1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL

LABORATORIES

EST. 1994

Shingles Pain

& Ulceration

Relief

TOPICAL HOMEOPATHIC SPRAY

1.0 FL OZ. (30 ml)

Shingles Pain & Ulceration Relief

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CALENDULA OFFICINALIS FLOWERING TOP	ACTIVE INGREDIENT	18E7415PXQ	2
CROTON TIGLIUM SEED	ACTIVE INGREDIENT	0HK2GZK66E	2
PLANTAGO MAJOR	ACTIVE INGREDIENT	W2469WNO6U	2
SMILAX REGELII ROOT	ACTIVE INGREDIENT	2H1576D5WG	2
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	2
TOXICODENDRON PUBESCENS LEAF	ACTIVE INGREDIENT	6IO182RP7A	2
CALENDULA OFFICINALIS FLOWERING TOP	ACTIVE MOIETY	18E7415PXQ	2
CHLORIDE ION	ACTIVE MOIETY	Q32ZN48698	2
CROTON TIGLIUM SEED	ACTIVE MOIETY	0HK2GZK66E	2
PLANTAGO MAJOR	ACTIVE MOIETY	W2469WNO6U	2
SARSAPARILLA	ACTIVE MOIETY	2H1576D5WG	2
TOXICODENDRON PUBESCENS LEAF	ACTIVE MOIETY	6IO182RP7A	2
.ALPHA.-TOCOPHEROL	INACTIVE INGREDIENT	H4N855PNZ1	2
ACHILLEA MILLEFOLIUM FLOWER	INACTIVE INGREDIENT	YQR8R0SQEA	2
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	2
ARNICA MONTANA	INACTIVE INGREDIENT	O80TY208ZW	2
ASCORBIC ACID	INACTIVE INGREDIENT	PQ6CK8PD0R	2
CAPRYLYL GLYCOL	INACTIVE INGREDIENT	00YIU5438U	2
COMFREY LEAF	INACTIVE INGREDIENT	DG4F8T839X	2
CROTON LECHLERI RESIN	INACTIVE INGREDIENT	GGG6W25C63	2
EGG SHELL MEMBRANE	INACTIVE INGREDIENT	N7QBR4212V	2
HYPERICUM PERFORATUM	INACTIVE INGREDIENT	XK4IUX8MNB	2
LARREA TRIDENTATA TOP	INACTIVE INGREDIENT	PK0TXD049P	2
LAVANDULA ANGUSTIFOLIA FLOWER	INACTIVE INGREDIENT	19AH1RAF4M	2
LECITHIN, SUNFLOWER	INACTIVE INGREDIENT	834K0WOS5G	2
MELISSA OFFICINALIS LEAF	INACTIVE INGREDIENT	50D2ZE9219	2
PEG-8 DIMETHICONE	INACTIVE INGREDIENT	GIA7T764OD	2
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	2
PHYTOLACCA AMERICANA FRUIT	INACTIVE INGREDIENT	WE63661499	2
PHYTOLACCA AMERICANA ROOT	INACTIVE INGREDIENT	11E6VI8VEG	2
POLYETHYLENE GLYCOL 1500	INACTIVE INGREDIENT	1212Z7S33A	2
POLYETHYLENE GLYCOL 700	INACTIVE INGREDIENT	762678AC5R	2
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	2
SALIX ALBA BARK	INACTIVE INGREDIENT	205MXS71H7	2
SILVER	INACTIVE INGREDIENT	3M4G523W1G	2
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	2
SORBIC ACID	INACTIVE INGREDIENT	X045WJ989B	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2
WHEY	INACTIVE INGREDIENT	8617Z5FMF6	2

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

SHINGLES PAIN ULCERATION RELIEF
Calendula officinalis, Croton tiglium, Natrum muriaticum, Plantago major, Rhus tox, Sarsaparilla (smilax regelii)
CALENDULA OFFICINALIS FLOWERING TOP
CROTON TIGLIUM SEED
SODIUM CHLORIDE
CHLORIDE ION
PLANTAGO MAJOR
TOXICODENDRON PUBESCENS LEAF
SMILAX REGELII ROOT
SARSAPARILLA
ALOE VERA LEAF
ARNICA MONTANA
LARREA TRIDENTATA TOP
COMFREY LEAF
CROTON LECHLERI RESIN
EGG SHELL MEMBRANE
LECITHIN, SUNFLOWER
LAVANDULA ANGUSTIFOLIA FLOWER
SILVER
MELISSA OFFICINALIS LEAF
POLYETHYLENE GLYCOL 1500
PEG-8 DIMETHICONE
POLYETHYLENE GLYCOL 700
PHENOXYETHANOL
CAPRYLYL GLYCOL
SORBIC ACID
PHYTOLACCA AMERICANA FRUIT
PHYTOLACCA AMERICANA ROOT
POTASSIUM SORBATE
WATER
SODIUM BICARBONATE
HYPERICUM PERFORATUM
.ALPHA.-TOCOPHEROL
ASCORBIC ACID
WHEY
SALIX ALBA BARK
ACHILLEA MILLEFOLIUM FLOWER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50845-0215	50845-0215-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CALENDULA OFFICINALIS FLOWERING TOP	18E7415PXQ	ACTIB
CROTON TIGLIUM SEED	0HK2GZK66E	ACTIB
SODIUM CHLORIDE	451W47IQ8X	ACTIB
PLANTAGO MAJOR	W2469WNO6U	ACTIB
TOXICODENDRON PUBESCENS LEAF	6IO182RP7A	ACTIB
SMILAX REGELII ROOT	2H1576D5WG	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
ARNICA MONTANA	O80TY208ZW	IACT
LARREA TRIDENTATA TOP	PK0TXD049P	IACT
COMFREY LEAF	DG4F8T839X	IACT
CROTON LECHLERI RESIN	GGG6W25C63	IACT
EGG SHELL MEMBRANE	N7QBR4212V	IACT
LECITHIN, SUNFLOWER	834K0WOS5G	IACT
LAVANDULA ANGUSTIFOLIA FLOWER	19AH1RAF4M	IACT
SILVER	3M4G523W1G	IACT
MELISSA OFFICINALIS LEAF	50D2ZE9219	IACT
POLYETHYLENE GLYCOL 1500	1212Z7S33A	IACT
PEG-8 DIMETHICONE	GIA7T764OD	IACT
POLYETHYLENE GLYCOL 700	762678AC5R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
CAPRYLYL GLYCOL	00YIU5438U	IACT
SORBIC ACID	X045WJ989B	IACT
PHYTOLACCA AMERICANA FRUIT	WE63661499	IACT
PHYTOLACCA AMERICANA ROOT	11E6VI8VEG	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
WATER	059QF0KO0R	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
HYPERICUM PERFORATUM	XK4IUX8MNB	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
ASCORBIC ACID	PQ6CK8PD0R	IACT
WHEY	8617Z5FMF6	IACT
SALIX ALBA BARK	205MXS71H7	IACT
ACHILLEA MILLEFOLIUM FLOWER	YQR8R0SQEA	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 2 · 119 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SORBIC ACID	SORBIC ACID	X045WJ989B	TABLET, FILM COATED / ORAL		5 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	AEROSOL, FOAM / TOPICAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	CONCENTRATE / ORAL	6 mg/1ml		Exact identifier — unii candidate 25 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	CAPSULE, DELAYED RELEASE / ORAL		12 mg	Exact identifier — unii candidate 25 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	0.11 %w/w		Exact identifier — unii candidate 25 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	LOTION / TOPICAL		4 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	SOLUTION / RESPIRATORY (INHALATION)	0.04 %w/w		Exact identifier — unii candidate 25 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	SOLUTION / RESPIRATORY (INHALATION)	2 %w/w		Exact identifier — unii candidate 34 equally ranked IID candidates
.ALPHA.-TOCOPHEROL	.ALPHA.-TOCOPHEROL	H4N855PNZ1	TABLET, CHEWABLE / ORAL	0.1 mg		Exact identifier — unii candidate 10 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET, EFFERVESCENT / ORAL		57600 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	INJECTION / INTRACAVITARY	5 mg		Exact identifier — unii candidate 25 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	GUM, CHEWING / ORAL		360 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET, CHEWABLE / ORAL	140 mg		Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	AEROSOL, FOAM / TOPICAL		8 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		6 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CREAM / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS		3219 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
.ALPHA.-TOCOPHEROL	.ALPHA.-TOCOPHEROL	H4N855PNZ1	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	0.64 mg		Exact identifier — unii candidate 10 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	CAPSULE, DELAYED RELEASE PELLETS / ORAL		4 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	TABLET / ORAL		10 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION / INTRAVENOUS	812 mg		Exact identifier — unii candidate 34 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	CREAM / TOPICAL		57 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	SOLUTION / ORAL	ADJ PH		Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET, ORALLY DISINTEGRATING / ORAL		107 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		3059 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	LOTION / TOPICAL	1 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	AEROSOL, METERED / RESPIRATORY (INHALATION)	0.1 %w/w		Exact identifier — unii candidate 25 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR	1000 mg		Exact identifier — unii candidate 34 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS		160 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
.ALPHA.-TOCOPHEROL	.ALPHA.-TOCOPHEROL	H4N855PNZ1	TABLET, EXTENDED RELEASE / ORAL		4 mg	Exact identifier — unii candidate 10 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	CAPSULE / ORAL		320 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	CREAM, AUGMENTED / TOPICAL		10 mg	Exact identifier — unii candidate 6 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET / BUCCAL		42 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	CAPSULE, EXTENDED RELEASE / ORAL		17 mg	Exact identifier — unii candidate 25 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	GRANULE, EFFERVESCENT / ORAL	267 mg		Exact identifier — unii candidate 34 equally ranked IID candidates
.ALPHA.-TOCOPHEROL	.ALPHA.-TOCOPHEROL	H4N855PNZ1	SYSTEM / TOPICAL	0.1 mg		Exact identifier — unii candidate 10 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	CONCENTRATE / ORAL		1 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	SYRUP / ORAL		80 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POLYETHYLENE GLYCOL 1500	POLYETHYLENE GLYCOL 1600	1212Z7S33A	PASTE / DENTAL	4.96 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	SOLUTION / ORAL		80 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	TABLET / ORAL		80 mg	Exact identifier — unii candidate 25 equally ranked IID candidates
.ALPHA.-TOCOPHEROL	.ALPHA.-TOCOPHEROL	H4N855PNZ1	TABLET, FILM COATED / ORAL		246 mg	Exact identifier — unii candidate 10 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	TABLET, COATED / ORAL	10.6 mg		Exact identifier — unii candidate 34 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	FILM, SOLUBLE / ORAL		2 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / RECTAL	6.67 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	SYRUP / ORAL		200 mg	Exact identifier — unii candidate 25 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	SUSPENSION / ORAL		520 mg	Exact identifier — unii candidate 25 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION / INTRAVITREAL	0.18 %w/v		Exact identifier — unii candidate 34 equally ranked IID candidates
PHENOXYETHANOL	PHENOXYETHANOL	HIE492ZZ3T	AEROSOL / TOPICAL	1.05 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
ASCORBIC ACID	ASCORBIC ACID	PQ6CK8PD0R	INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS	2 mg		Exact identifier — unii candidate 25 equally ranked IID candidates
SORBIC ACID	SORBIC ACID	X045WJ989B	TABLET, FILM COATED, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM BICARBONATE	SODIUM BICARBONATE	8MDF5V39QO	INJECTION / INTRAMUSCULAR		175 mg	Exact identifier — unii candidate 34 equally ranked IID candidates
POLYETHYLENE GLYCOL 1500	POLYETHYLENE GLYCOL 1600	1212Z7S33A	SUPPOSITORY / RECTAL	0.3 mg/mg		Exact identifier — unii candidate 6 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
25e77349-98a9-4c96-aab7-51b8178fd9c3			149171e7-8dd2-44ef-8986-e8fcc9ea8422	2018-05-10	Warnings	Exact identifier spl id: 25e77349-98a9-4c96-aab7-51b8178fd9c3 spl set id: 149171e7-8dd2-44ef-8986-e8fcc9ea8422

Reported adverse events (FAERS/openFDA)#

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