Bug Away

Manufacturer: King Bio Inc.
Effective date: 2015-03-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:06:31

Label at a glance#

ProductBug Away

Active ingredientAPIS MELLIFERA, HELIANTHEMUM CANADENSE, ANHYDROUS CITRIC ACID, HYPERICUM PERFORATUM, POTASSIUM NITRATE, LEDUM PALUSTRE TWIG, LYCOPODIUM CLAVATUM SPORE, DAPHNE MEZEREUM BARK, PULEX IRRITANS, PULSATILLA VULGARIS, DELPHINIUM STAPHISAGRIA SEED, SULFUR, URTICA URENS

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts__________________________________________________________________________________________________________

HPUS active ingredients: Apis mellifica, Cistus canadensis, Citricum acidum, Hypericum perforatum, Kali nitricum, Ledum palustre, Lycopodium clavatum, Mezereum, Pulex irritans, Pulsatilla, Staphysagria, Sulphur, Urtica Urens. Equal volumes of each ingredient in 10X, 30X, 100X, 1M, LM1, LM2, LM3 potencies.

INDICATIONS & USAGE SECTION

Uses temporarily relieves symptoms of insect bites and stings: itching, swelling, irritations, discomforts, redness, burning pain.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

WARNINGS SECTION

Warnings

Stop use and ask your doctor if symptoms persist or worsen.
If pregnant or breast-feeding, take only on advice of a healthcare professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Initially, depress pump until primed.
Spray one dose directly into mouth.
Adults: 3 sprays 3 times per day
Children 2-12 years: 2 sprays 3 times per day.
Use additionally as needed, up to 6 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if safety seal is intact.

OTC - PURPOSE SECTION

Uses temporarily relieves symptoms of insect bites and stings:

itching
swelling
irritations
discomforts
redness
burning pain

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
57955-0077-2	2020-01-31	C162847	48780-1	9d75b9d0-5ab5-f424-e053-dadaa90a57ce	Bug Away

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
57955-0077-2	Bug Away	59 mL in 1 BOTTLE, SPRAY	LIQUID	59		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57955-0077	BUG AWAY (APIS MELLIFICA, CISTUS CANADENSIS, CITRICUM ACIDUM, HYPERICUM PERFORATUM, KALI NITRICUM, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, MEZEREUM, PULEX IRRITANS, PULSATILLA, STAPHYSAGRIA, SULPHUR, URTICA URENS) LIQUID [KING BIO INC.]	1	Legacy NDC, 1 package rows	20150306_f116c32a-c1e8-4059-af6c-a79e56445b19.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ANHYDROUS CITRIC ACID	ACTIVE INGREDIENT	XF417D3PSL	1
APIS MELLIFERA	ACTIVE INGREDIENT	7S82P3R43Z	1
DAPHNE MEZEREUM BARK	ACTIVE INGREDIENT	X2N6E405GV	1
DELPHINIUM STAPHISAGRIA SEED	ACTIVE INGREDIENT	00543AP1JV	1
HELIANTHEMUM CANADENSE	ACTIVE INGREDIENT	46G3W789Q3	1
HYPERICUM PERFORATUM	ACTIVE INGREDIENT	XK4IUX8MNB	1
LEDUM PALUSTRE TWIG	ACTIVE INGREDIENT	877L01IZ0P	1
LYCOPODIUM CLAVATUM SPORE	ACTIVE INGREDIENT	C88X29Y479	1
POTASSIUM NITRATE	ACTIVE INGREDIENT	RU45X2JN0Z	1
PULEX IRRITANS	ACTIVE INGREDIENT	L63DD62R8R	1
PULSATILLA VULGARIS	ACTIVE INGREDIENT	I76KB35JEV	1
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	1
URTICA URENS	ACTIVE INGREDIENT	IHN2NQ5OF9	1
ANHYDROUS CITRIC ACID	ACTIVE MOIETY	XF417D3PSL	1
APIS MELLIFERA	ACTIVE MOIETY	7S82P3R43Z	1
DAPHNE MEZEREUM BARK	ACTIVE MOIETY	X2N6E405GV	1
DELPHINIUM STAPHISAGRIA SEED	ACTIVE MOIETY	00543AP1JV	1
HELIANTHEMUM CANADENSE	ACTIVE MOIETY	46G3W789Q3	1
HYPERICUM PERFORATUM	ACTIVE MOIETY	XK4IUX8MNB	1
LEDUM PALUSTRE TWIG	ACTIVE MOIETY	877L01IZ0P	1
LYCOPODIUM CLAVATUM SPORE	ACTIVE MOIETY	C88X29Y479	1
NITRATE ION	ACTIVE MOIETY	T93E9Y2844	1
PULEX IRRITANS	ACTIVE MOIETY	L63DD62R8R	1
PULSATILLA VULGARIS	ACTIVE MOIETY	I76KB35JEV	1
SULFUR	ACTIVE MOIETY	70FD1KFU70	1
URTICA URENS	ACTIVE MOIETY	IHN2NQ5OF9	1
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

Bug Away
Apis mellifica, Cistus canadensis, Citricum acidum, Hypericum perforatum, Kali nitricum, Ledum palustre, Lycopodium clavatum, Mezereum, Pulex irritans, Pulsatilla, Staphysagria, Sulphur, Urtica urens
APIS MELLIFERA
HELIANTHEMUM CANADENSE
ANHYDROUS CITRIC ACID
HYPERICUM PERFORATUM
POTASSIUM NITRATE
NITRATE ION
LEDUM PALUSTRE TWIG
LYCOPODIUM CLAVATUM SPORE
DAPHNE MEZEREUM BARK
PULEX IRRITANS
PULSATILLA VULGARIS
DELPHINIUM STAPHISAGRIA SEED
SULFUR
URTICA URENS
WATER
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
57955-0077	57955-0077-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
APIS MELLIFERA	7S82P3R43Z	ACTIB
HELIANTHEMUM CANADENSE	46G3W789Q3	ACTIB
ANHYDROUS CITRIC ACID	XF417D3PSL	ACTIB
HYPERICUM PERFORATUM	XK4IUX8MNB	ACTIB
POTASSIUM NITRATE	RU45X2JN0Z	ACTIB
LEDUM PALUSTRE TWIG	877L01IZ0P	ACTIB
LYCOPODIUM CLAVATUM SPORE	C88X29Y479	ACTIB
DAPHNE MEZEREUM BARK	X2N6E405GV	ACTIB
PULEX IRRITANS	L63DD62R8R	ACTIB
PULSATILLA VULGARIS	I76KB35JEV	ACTIB
DELPHINIUM STAPHISAGRIA SEED	00543AP1JV	ACTIB
SULFUR	70FD1KFU70	ACTIB
URTICA URENS	IHN2NQ5OF9	ACTIB
WATER	059QF0KO0R	IACT
POTASSIUM SORBATE	1VPU26JZZ4	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 · 19 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	EMULSION / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SPRAY, METERED / NASAL	0.06 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / RECTAL	6.67 %w/v		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
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	LOTION / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii candidate 19 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
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	AEROSOL, FOAM / TOPICAL		8 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CREAM / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION/ DROPS / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii candidate 19 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
d8219764-299b-4954-8e9e-6b96c2c6d38a			f116c32a-c1e8-4059-af6c-a79e56445b19	2015-03-06	Warnings	Exact identifier spl id: d8219764-299b-4954-8e9e-6b96c2c6d38a spl set id: f116c32a-c1e8-4059-af6c-a79e56445b19

Reported adverse events (FAERS/openFDA)#

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