Triple Allergy Defense

Manufacturer: Nenningers Naturals, LLC | King Bio, Inc.
Effective date: 2013-03-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:04:23

Label at a glance#

ProductTriple Allergy Defense

Active ingredientALLIUM CEPA WHOLE, AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LEMNA MINOR, FLAX SEED, LUFFA OPERCULATA FRUIT, SODIUM CHLORIDE, FOMITOPSIS PINICOLA FRUITING BODY, SCHOENOCAULON OFFICINALE SEED

Label structure9 sections

Contacts and useful links#

PhoneLabel contact(888) 770-1925

Websitewww.tripleallergydefense.com

www.TripleAllergyDefense.com

Label contents#

Full prescribing information#

Drug Facts

OTC - PURPOSE SECTION

Purpose: To reduce the duration and severity of allergy symptoms related to pollen, mold and dust.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Nenninger

TRIPLE

ALLERGY

DEFENSE

Pollen, Mold, Dust

Homeopathic Allergy Relief

2 Fluid Ounces/60 ml

Triple Allergy Defense 60 ml Label

OTC - QUESTIONS SECTION

Nenningers Naturals, LLC

East Setauket, NY 11733

Questions/Comments (888) 770-1925

www.TripleAllergyDefense.com

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

OTC - DO NOT USE SECTION

Do not use if safety seal at neck of bottle is broken or missing.

OTC - ASK DOCTOR SECTION

If symptoms worsen or persist for more than 7 days seek advice from physician.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding consult a healthcare professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions: Take 1-3 times per day as

needed. Adult Dose is 20 drops. Children

under 12 take 2 drops for every 10 pounds

of body weight up to a maximum of 20

drops. Place drops on tongue or mix with

1 oz. of water.

INDICATIONS & USAGE SECTION

Uses: Multi-symptom allergy relief for

sneezing, runny nose, nasal and sinus

congestion, cough, itchy and watery

eyes, headache, fatigue.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic grape

alcohol 15%, purified water

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: HPUS*

Allium cepa 30c, Ambrosia artemisiaefolia 30c,

Arsenicum album 30c, Euphrasia officinalis 30c,

Galphimia glauca 30c, Histaminum

hydrochloricum 30c, Lemna minor 30c,

Linum usitatissimum 30c, Luffa operculata 30c,

Natrum muriaticum 30c, Polyporus

pinicola 30c, Sabadilla 30c

*HPUS indicates official Homeopathic

Pharmacopeia of the United States

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
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
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
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
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
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
42731-002-02	2020-01-31	C162847	48780-1	9d75b9cf-d856-f424-e053-dadaa90a57ce	Dr. Nenninger Triple Allergy Defense

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
42731-002-02	Triple Allergy Defense	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42731-002	TRIPLE ALLERGY DEFENSE (ALLIUM CEPA, AMRBOSIA ARTEMISIIFOLIA, ARSENICUM ALBUM, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, LEMNA MINOR, LINUM USITATISSIMUM, LUFFA OPERCULATA, NATRUM MURIATICUM, POLYPORUS PINICOLA, SABADILLA) LIQUID [NENNINGERS NATURALS, LLC]	1	Legacy NDC, 1 package rows	20130313_bf17a6eb-e542-4c5a-90e1-a85e5f83835b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALLIUM CEPA WHOLE	ACTIVE INGREDIENT	8P2VLG2456	1
AMBROSIA ARTEMISIIFOLIA	ACTIVE INGREDIENT	9W34L2CQ9A	1
ARSENIC TRIOXIDE	ACTIVE INGREDIENT	S7V92P67HO	1
EUPHRASIA STRICTA	ACTIVE INGREDIENT	C9642I91WL	1
FLAX SEED	ACTIVE INGREDIENT	4110YT348C	1
FOMITOPSIS PINICOLA FRUITING BODY	ACTIVE INGREDIENT	30D02U2IRN	1
GALPHIMIA GLAUCA FLOWERING TOP	ACTIVE INGREDIENT	93PH5Q8M7E	1
HISTAMINE DIHYDROCHLORIDE	ACTIVE INGREDIENT	3POA0Q644U	1
LEMNA MINOR	ACTIVE INGREDIENT	621HHM46SV	1
LUFFA OPERCULATA FRUIT	ACTIVE INGREDIENT	C4MO6809HU	1
SCHOENOCAULON OFFICINALE SEED	ACTIVE INGREDIENT	6NAF1689IO	1
SODIUM CHLORIDE	ACTIVE INGREDIENT	451W47IQ8X	1
ALLIUM CEPA WHOLE	ACTIVE MOIETY	8P2VLG2456	1
AMBROSIA ARTEMISIIFOLIA	ACTIVE MOIETY	9W34L2CQ9A	1
ARSENIC CATION (3+)	ACTIVE MOIETY	C96613F5AV	1
CHLORIDE ION	ACTIVE MOIETY	Q32ZN48698	1
EUPHRASIA STRICTA	ACTIVE MOIETY	C9642I91WL	1
FLAX SEED	ACTIVE MOIETY	4110YT348C	1
FOMITOPSIS PINICOLA FRUITING BODY	ACTIVE MOIETY	30D02U2IRN	1
GALPHIMIA GLAUCA FLOWERING TOP	ACTIVE MOIETY	93PH5Q8M7E	1
HISTAMINE	ACTIVE MOIETY	820484N8I3	1
LEMNA MINOR	ACTIVE MOIETY	621HHM46SV	1
LUFFA OPERCULATA FRUIT	ACTIVE MOIETY	C4MO6809HU	1
SCHOENOCAULON OFFICINALE SEED	ACTIVE MOIETY	6NAF1689IO	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

Triple Allergy Defense
Allium cepa, Amrbosia artemisiifolia, Arsenicum album, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Lemna minor, Linum usitatissimum, Luffa operculata, Natrum muriaticum, Polyporus pinicola, Sabadilla
ALLIUM CEPA WHOLE
AMBROSIA ARTEMISIIFOLIA
ARSENIC TRIOXIDE
ARSENIC CATION (3+)
EUPHRASIA STRICTA
GALPHIMIA GLAUCA FLOWERING TOP
HISTAMINE DIHYDROCHLORIDE
HISTAMINE
LEMNA MINOR
FLAX SEED
LUFFA OPERCULATA FRUIT
SODIUM CHLORIDE
CHLORIDE ION
FOMITOPSIS PINICOLA FRUITING BODY
SCHOENOCAULON OFFICINALE SEED
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42731-002	42731-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALLIUM CEPA WHOLE	8P2VLG2456	ACTIB
AMBROSIA ARTEMISIIFOLIA	9W34L2CQ9A	ACTIB
ARSENIC TRIOXIDE	S7V92P67HO	ACTIM
EUPHRASIA STRICTA	C9642I91WL	ACTIB
GALPHIMIA GLAUCA FLOWERING TOP	93PH5Q8M7E	ACTIB
HISTAMINE DIHYDROCHLORIDE	3POA0Q644U	ACTIB
LEMNA MINOR	621HHM46SV	ACTIB
FLAX SEED	4110YT348C	ACTIB
LUFFA OPERCULATA FRUIT	C4MO6809HU	ACTIB
SODIUM CHLORIDE	451W47IQ8X	ACTIB
FOMITOPSIS PINICOLA FRUITING BODY	30D02U2IRN	ACTIB
SCHOENOCAULON OFFICINALE SEED	6NAF1689IO	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	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 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / INTRAVENOUS		4000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVENOUS	92 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / RECTAL		898 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SWAB / TOPICAL		2250 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	POWDER, FOR SOLUTION / TOPICAL	40 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / NASAL	70 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / BUCCAL	679 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / RESPIRATORY (INHALATION)	0.08 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	PASTE / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TRANSDERMAL		7360 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAMUSCULAR		1491 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / SUBCUTANEOUS		149 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, FOAM / TOPICAL		4504 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAMUSCULAR		1000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAVENOUS		6405 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAVENOUS		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVASCULAR	100 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	35.75 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVESICAL		7892 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAMUSCULAR		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TOPICAL		9971 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TRANSDERMAL	49.37 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	JELLY / VAGINAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVENOUS		99 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TRANSDERMAL		3675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / NASAL	20 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / RESPIRATORY (INHALATION)		26664 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY, METERED / SUBLINGUAL		29 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / DENTAL	12.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TOPICAL		541 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, EMULSION / INTRAVENOUS		520 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SHAMPOO / TOPICAL		714 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / SUBCUTANEOUS	6.1 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / RECTAL	0.35 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	MOUTHWASH / BUCCAL	200 mg/1ml		Exact identifier — unii candidate 59 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
774be21f-b325-4a3a-8714-87b92dcc94b1			bf17a6eb-e542-4c5a-90e1-a85e5f83835b	2013-03-12	Warnings	Exact identifier spl id: 774be21f-b325-4a3a-8714-87b92dcc94b1 spl set id: bf17a6eb-e542-4c5a-90e1-a85e5f83835b

Reported adverse events (FAERS/openFDA)#

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