FDA.reportPublic FDA data

Additive and Preservative Detox

Manufacturer
King Bio Inc.
Effective date
2011-11-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:23

Label at a glance#

ProductAdditive and Preservative Detox
Active ingredientFORMIC ACID, GAMBOGE, SODIUM BICARBONATE, SODIUM NITRATE, SODIUM NITRITE, SODIUM SULFITE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PHYTOLACCA AMERICANA ROOT, SACCHARIN
Label structure8 sections

Indications and uses

Uses for temporary relief of symptoms from food additives and preservatives: gastrointestinal upset, hives, itching, nasal congestion, hyperactivity, muscle weakness, headaches, difficulty sleeping, irritability. Reference image detox.jpg

Dosage and administration

Directions Initially, depress pump until primed. Hold close to mouth and spray one dose directly into mouth. Use 3 times per day. Use additionally as needed. Adult Dose: 3 pump sprays Children 2 - 12 years: 2 pump sprays Reference image detox.jpg

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Official HPUS:

Formicum Acidum

Gambogia

Natrum Bicarbonicum

Natrum Nitricum

Natrum Nitrosum

Natrum Sulphurosum

Nux Vomica

Phosphoricum Acidum

Phytolacca Decandra

Saccharinum

Reference image detox.jpg

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base:12X, 24X and LM1 Potencies.

Reference image detox.jpg

Purpose

OTC - PURPOSE SECTION

Uses for temporary relief of symptoms from food additives and preservatives:

  • gastrointestinal upset
  • hives
  • itching
  • nasal congestion
  • hyperactivity
  • muscle weakness
  • headaches
  • difficulty sleeping
  • irritability
Reference image detox.jpg

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Directions Initially, depress pump until primed. Hold close to mouth and spray one dose directly into mouth. Use 3 times per day. Use additionally as needed.

Adult Dose: 3 pump sprays

Children 2 - 12 years: 2 pump sprays

Reference image detox.jpg

Warnings

WARNINGS SECTION

If symptoms persist or worsen, or if pregnant or nursing, take only on advice of a healthcare professional. Keep out of reach of children.

Reference image detox.jpg

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Reference image detox.jpg

Indications and usage

INDICATIONS & USAGE SECTION

Uses for temporary relief of symptoms from food additives and preservatives: gastrointestinal upset, hives, itching, nasal congestion, hyperactivity, muscle weakness, headaches, difficulty sleeping, irritability.

Reference image detox.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of label
Image of label

King Bio Inc.

3 Westside Drive

Asheville, NC 28806

Questions? Call 800.543.3245

www.kingbio.com

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
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fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
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9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
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419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
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08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
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5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-6205-22020-01-31C16284748780-19d75b9d0-b560-f424-e053-dadaa90a57ceAdditive and Preservative Detox

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-6205-2Additive and Preservative Detox59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-6205ADDITIVE AND PRESERVATIVE DETOX (NATURAL MEDICINE) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20111117_cc46b3e6-5608-4c6d-912a-e2ed5a31ad4d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FORMIC ACIDACTIVE INGREDIENT0YIW783RG11
GAMBOGEACTIVE INGREDIENT7556HJ75871
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG1
SACCHARINACTIVE INGREDIENTFST467XS7D1
SODIUM BICARBONATEACTIVE INGREDIENT8MDF5V39QO1
SODIUM NITRATEACTIVE INGREDIENT8M4L3H2ZVZ1
SODIUM NITRITEACTIVE INGREDIENTM0KG633D4F1
SODIUM SULFITEACTIVE INGREDIENTVTK01UQK3G1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
FORMIC ACIDACTIVE MOIETY0YIW783RG11
GAMBOGEACTIVE MOIETY7556HJ75871
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG1
SACCHARINACTIVE MOIETYFST467XS7D1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-620557955-6205-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
FORMIC ACID0YIW783RG1ACTIB
GAMBOGE7556HJ7587ACTIB
SODIUM BICARBONATE8MDF5V39QOACTIB
SODIUM NITRATE8M4L3H2ZVZACTIB
SODIUM NITRITEM0KG633D4FACTIB
SODIUM SULFITEVTK01UQK3GACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
SACCHARINFST467XS7DACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7d5a865d-261a-4a43-a273-f1b7da106e03cc46b3e6-5608-4c6d-912a-e2ed5a31ad4d2011-11-16WarningsExact identifier
spl id: 7d5a865d-261a-4a43-a273-f1b7da106e03
spl set id: cc46b3e6-5608-4c6d-912a-e2ed5a31ad4d

Reported adverse events (FAERS/openFDA)#

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