GUNA-SINUS NOSE SPRAY

Manufacturer: Guna spa
Effective date: 2018-12-22
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:11:13

Label at a glance#

ProductGUNA-SINUS NOSE

Active ingredientONION, ALTHAEA OFFICINALIS LEAF, SILVER NITRATE, ASCORBIC ACID, BLACK CURRANT, LOBARIA PULMONARIA, COPPER, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, MANGANESE, MERCURIC SULFIDE, SUS SCROFA NASAL MUCOSA, PLANTAGO MAJOR, PULSATILLA VULGARIS, SILICON DIOXIDE, SINUSITISINUM, SUS SCROFA THYMUS, SUS SCROFA URINARY BLADDER

Label structure10 sections

Indications and uses

For the temporary relief of symptoms due to acute and chronic Sinus Infection: Sinus Headaches Post Nasal Drip Nasal Congestion

Dosage and administration

Adults and children 12 years and older 2 sprays to each nostril, 3-5 times per day Children between 12 years and 6 years of age 1 spray to each nostril, 3-5 times per day Children under 6 years 1 spray to each nostril, 3 times per day

Contacts and useful links#

PhoneLabel contact(484) 223-3500

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

ALIUM CEPA 6X, 8X, 12X EXPECTORANT

ALTHEA OFFICINALIS 2X EXPECTORANT

ARGENTUM NITRICUM 10X HEADACHE ANALGESIC

ASCORBIC ACID 2X ANTIOXIDANT

BLACK CURRANT 1X DETOXIFICATION

COMMON LUNGWORT 2X DECONGESTANT

CUPRUM METALLICUM 3X ANTIVIRAL IMMUNE SUPPORT

ECHINACEA ANGUSTIFOLIA 3X ANTIBACTERIAL IMMUNE SUPPORT

HEPAR SULFURIS CALCAREUM 6X, 8X, 12X ANTIOXIDANT

HYDRASTIS CANADENSIS 6X, 8X, 12X MUCOLYTIC

KALI BICHROMICUM 6X, 8X, 12X MUCOLYTIC

LACHESIS MUTUS 12X, 30X, 200X DECONGESTANT

MANGANUM METALLICUM 3X DECONGESTANT

MERCURIUS SULPHURATUS RUBER 6X, 8X, 12X ANTI-INFLAMMATORY

MUCOSA NASALIS 6X, 12X, 30X SUPPORTS IMMUNE RESPONSE

PLANTAGO MAJOR 2X DETOXIFICATION

PULSATILLA 6X, 8X, 12X DECONGESTANT

SILICEA 6X, 8X, 12X DECONGESTANT

SINUSITISINUM 12X, 30X DECONGESTANT

THYMUS GLAND 6X, 12X, 30X SUPPORTS IMMUNE RESPONSE

URINARY BLADDER 10X, 30X, 200X DETOXIFICATION

USES

OTC - PURPOSE SECTION

For the temporary relief of symptoms due to acute and chronic Sinus Infection:

Sinus Headaches
Post Nasal Drip
Nasal Congestion

WARNINGS

WARNINGS SECTION

Stop use and ask doctor if symptoms persist more than 5 days.
If pregnant or breast-feeding ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a doctor before use

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older 2 sprays to each nostril, 3-5 times per day

Children between 12 years and 6 years of age 1 spray to each nostril, 3-5 times per day

Children under 6 years 1 spray to each nostril, 3 times per day

QUESTIONS

OTC - QUESTIONS SECTION

Questions?: info@gunainc.com
Tel. (484) 223-3500

INACTIVE INGREDIENT SECTION

Inactive ingredient: orange juice, potassium sorbate, sodium benzoate, water.

INDICATIONS & USAGE SECTION

Directions:

tilt head slightly forward, place tip of bottle into nose, compress bottle once for each spray, aiming towards the back of the nose.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 5USSIN-Rev06-11-05-18

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124
c5cd4727-ac49-4409-82b1-5bd8006c3ec7	Product name	1	20171122
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
17089-451-23	GUNA-SINUS NOSE	30 mL in 1 BOTTLE, SPRAY	SPRAY	30		3
17089-451-23	GUNA-SINUS NOSE	1 in 1 BOX	SPRAY	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17089-451	GUNA-SINUS NOSE (ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER -) SPRAY [GUNA SPA]	3	Current NDC, Legacy NDC, 2 package rows	20190404_36fef678-17c6-4d2a-a0f0-ddb298611f25.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALTHAEA OFFICINALIS LEAF	ACTIVE INGREDIENT	E2QQV92338	2
ASCORBIC ACID	ACTIVE INGREDIENT	PQ6CK8PD0R	2
BLACK CURRANT	ACTIVE INGREDIENT	9755T40D11	2
CALCIUM SULFIDE	ACTIVE INGREDIENT	1MBW07J51Q	2
COPPER	ACTIVE INGREDIENT	789U1901C5	2
ECHINACEA ANGUSTIFOLIA	ACTIVE INGREDIENT	VB06AV5US8	2
GOLDENSEAL	ACTIVE INGREDIENT	ZW3Z11D0JV	2
LACHESIS MUTA VENOM	ACTIVE INGREDIENT	VSW71SS07I	2
LOBARIA PULMONARIA	ACTIVE INGREDIENT	D1YM0P5Z2T	2
MANGANESE	ACTIVE INGREDIENT	42Z2K6ZL8P	2
MERCURIC SULFIDE	ACTIVE INGREDIENT	ZI0T668SF1	2
ONION	ACTIVE INGREDIENT	492225Q21H	2
PLANTAGO MAJOR	ACTIVE INGREDIENT	W2469WNO6U	2
POTASSIUM DICHROMATE	ACTIVE INGREDIENT	T4423S18FM	2
PULSATILLA VULGARIS	ACTIVE INGREDIENT	I76KB35JEV	2
SILICON DIOXIDE	ACTIVE INGREDIENT	ETJ7Z6XBU4	2
SILVER NITRATE	ACTIVE INGREDIENT	95IT3W8JZE	2
SINUSITISINUM	ACTIVE INGREDIENT	B575563DM5	2
SUS SCROFA NASAL MUCOSA	ACTIVE INGREDIENT	ID3Z1X61WY	2
SUS SCROFA THYMUS	ACTIVE INGREDIENT	7B69B0BD62	2
SUS SCROFA URINARY BLADDER	ACTIVE INGREDIENT	3G7U72W8DA	2
ALTHAEA OFFICINALIS LEAF	ACTIVE MOIETY	E2QQV92338	2
ASCORBIC ACID	ACTIVE MOIETY	PQ6CK8PD0R	2
BLACK CURRANT	ACTIVE MOIETY	9755T40D11	2
CALCIUM CATION	ACTIVE MOIETY	2M83C4R6ZB	2
COPPER	ACTIVE MOIETY	789U1901C5	2
ECHINACEA ANGUSTIFOLIA	ACTIVE MOIETY	VB06AV5US8	2
GOLDENSEAL	ACTIVE MOIETY	ZW3Z11D0JV	2
LACHESIS MUTA VENOM	ACTIVE MOIETY	VSW71SS07I	2
LOBARIA PULMONARIA	ACTIVE MOIETY	D1YM0P5Z2T	2
MANGANESE	ACTIVE MOIETY	42Z2K6ZL8P	2
MERCURIC CATION	ACTIVE MOIETY	ED30FJ8Y42	2
ONION	ACTIVE MOIETY	492225Q21H	2
PLANTAGO MAJOR	ACTIVE MOIETY	W2469WNO6U	2
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	2
PULSATILLA VULGARIS	ACTIVE MOIETY	I76KB35JEV	2
SILICON DIOXIDE	ACTIVE MOIETY	ETJ7Z6XBU4	2
SILVER CATION	ACTIVE MOIETY	57N7B0K90A	2
SINUSITISINUM	ACTIVE MOIETY	B575563DM5	2
SUS SCROFA NASAL MUCOSA	ACTIVE MOIETY	ID3Z1X61WY	2
SUS SCROFA THYMUS	ACTIVE MOIETY	7B69B0BD62	2
SUS SCROFA URINARY BLADDER	ACTIVE MOIETY	3G7U72W8DA	2
ORANGE JUICE	INACTIVE INGREDIENT	5A9KE2L9L3	2
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	2
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

GUNA-SINUS NOSE
ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER -
ORANGE JUICE
POTASSIUM SORBATE
WATER
SODIUM BENZOATE
ONION
ALTHAEA OFFICINALIS LEAF
SILVER NITRATE
SILVER CATION
ASCORBIC ACID
BLACK CURRANT
LOBARIA PULMONARIA
COPPER
ECHINACEA ANGUSTIFOLIA
CALCIUM SULFIDE
GOLDENSEAL
POTASSIUM DICHROMATE
DICHROMATE ION
LACHESIS MUTA VENOM
MANGANESE
MERCURIC SULFIDE
MERCURIC CATION
SUS SCROFA NASAL MUCOSA
PLANTAGO MAJOR
PULSATILLA VULGARIS
SILICON DIOXIDE
SINUSITISINUM
SUS SCROFA THYMUS
SUS SCROFA URINARY BLADDER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
17089-451	17089-451-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ORANGE JUICE	5A9KE2L9L3	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
WATER	059QF0KO0R	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
ONION	492225Q21H	ACTIB
ALTHAEA OFFICINALIS LEAF	E2QQV92338	ACTIB
SILVER NITRATE	95IT3W8JZE	ACTIB
ASCORBIC ACID	PQ6CK8PD0R	ACTIB
BLACK CURRANT	9755T40D11	ACTIB
LOBARIA PULMONARIA	D1YM0P5Z2T	ACTIB
COPPER	789U1901C5	ACTIB
ECHINACEA ANGUSTIFOLIA	VB06AV5US8	ACTIB
CALCIUM SULFIDE	1MBW07J51Q	ACTIB
GOLDENSEAL	ZW3Z11D0JV	ACTIB
POTASSIUM DICHROMATE	T4423S18FM	ACTIB
LACHESIS MUTA VENOM	VSW71SS07I	ACTIB
MANGANESE	42Z2K6ZL8P	ACTIB
MERCURIC SULFIDE	ZI0T668SF1	ACTIB
SUS SCROFA NASAL MUCOSA	ID3Z1X61WY	ACTIB
PLANTAGO MAJOR	W2469WNO6U	ACTIB
PULSATILLA VULGARIS	I76KB35JEV	ACTIB
SILICON DIOXIDE	ETJ7Z6XBU4	ACTIB
SINUSITISINUM	B575563DM5	ACTIB
SUS SCROFA THYMUS	7B69B0BD62	ACTIB
SUS SCROFA URINARY BLADDER	3G7U72W8DA	ACTIB

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 · 74 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	POWDER, FOR SOLUTION / ORAL		98 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	POWDER, FOR SUSPENSION / ORAL		160 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION / INTRAMUSCULAR		864 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	PASTE, DENTIFRICE / DENTAL	0.5 %w/w		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SPONGE / TOPICAL	NA		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	FILM / BUCCAL		1 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, COATED / ORAL	0.2 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SOLUTION / ORAL		660 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii+route 2 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SYSTEM / TOPICAL		2 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	ELIXIR / ORAL	5.02 mg/5ml		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	FILM, SOLUBLE / BUCCAL		3 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, DELAYED RELEASE / ORAL	0.34 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SOLUTION / ORAL		660 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	ELIXIR / ORAL	5.02 mg/5ml		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SYRUP / ORAL		80 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	PASTE / DENTAL	0.08 %w/w		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	PASTE / ORAL		28 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
ORANGE JUICE	ORANGE JUICE	5A9KE2L9L3	SOLUTION / ORAL	NA		Exact identifier — unii candidate 2 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION / INTRAMUSCULAR		864 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GRANULE, EFFERVESCENT / ORAL	60 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, COATED / ORAL	0.2 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	POWDER, FOR SOLUTION / ORAL		98 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, FILM COATED / ORAL		1 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CAPSULE / ORAL	8.5 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SUSPENSION, EXTENDED RELEASE / ORAL		24 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	ENEMA / RECTAL		60 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SUSPENSION / ORAL		320 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION, SOLUTION / INTRAMUSCULAR	4.8 %w/v		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET / ORAL	30 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CONCENTRATE / ORAL		20 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CREAM / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET / ORAL	30 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CAPSULE / ORAL	8.5 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SOLUTION / TOPICAL	0.1 %w/v		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION / INTRAVENOUS		864 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GRANULE, FOR SUSPENSION / ORAL		120 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SUSPENSION, EXTENDED RELEASE / ORAL		24 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION, EMULSION / INTRAVENOUS	0.1 %w/v		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GRANULE / ORAL	NA		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	FILM / BUCCAL		1 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GEL / TOPICAL		5 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION, SOLUTION / INTRAMUSCULAR	4.8 %w/v		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, FILM COATED / ORAL		1 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	FILM, SOLUBLE / BUCCAL		3 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GEL / RECTAL		406 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	PASTE / DENTAL	0.08 %w/w		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SUSPENSION/ DROPS / ORAL		23 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SUSPENSION / ORAL		320 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	PASTE / ORAL		28 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	SYRUP / ORAL		80 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GRANULE, FOR SUSPENSION / ORAL		120 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CONCENTRATE / ORAL		20 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	INJECTION / INTRAVENOUS		864 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	CREAM / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	TABLET, DELAYED RELEASE / ORAL	0.34 mg		Exact identifier — unii candidate 70 equally ranked IID candidates
SODIUM BENZOATE	SODIUM BENZOATE	OJ245FE5EU	GEL / TOPICAL		5 mg	Exact identifier — unii candidate 70 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii+route 2 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
GUNA-SINUS NOSE	ALTHAEA OFFICINALIS LEAF - ASCORBIC ACID - BLACK CURRANT - CALCIUM SULFIDE - COPPER - ECHINACEA ANGUSTIFOLIA - GOLDENSEAL - LACHESIS MUTA VENOM - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR - POTASSIUM CARBONATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA - SUS SCROFA THYMUS - SUS SCROFA URINARY BLADDER -	Guna spa	36fef678-17c6-4d2a-a0f0-ddb298611f25	2018-12-22	Warnings	Exact identifier ndc (package): 17089-451-23 ndc (product): 17089-451 ndc11 (package): 17089045123 spl id: 7d9d997a-fda9-2a63-e053-2a91aa0a0000 spl set id: 36fef678-17c6-4d2a-a0f0-ddb298611f25

Reported adverse events (FAERS/openFDA)#

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