Dosage and administration
3 to 10 drops under the tongue 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
3 to 10 drops under the tongue 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Adenosinum Triphosphoricum Dinatrum 4X, Acetaldehyde 6X, 8X, 12X, 30X, 200X, Cinnamic Acid 6X, 8X, 12X, 30X, 200X, Gallicum Acidum 6X, 8X, 12X, 30X, 200X, Hesperidin 6X, 8X, 12X, 30X, 200X, Malvin (Chloride) 6X, 8X, 12X, 30X, 200X, Quercetin 6X, 8X, 12X, 30X, 200X, Rutin 6X, 8X, 12X, 30X, 200X, Ileum (Suis) 8X, Jejunum (Suis) 8X, Stomach (Suis) 8X, Chlorophyllin 10X, 30X, Aceticum Acidum 6C, 30C, 200C, Arsenicum Album 6C, 30C, 200C, Ascorbic Acid 6C, 30C, 200C, Belladonna 6C, 30C, 200C, Oxalicum Acidum 6C, 30C, 200C, Sarcolacticum Acidum 6C, 30C, 200C, Adrenocorticotrophin 8C, 30C, 200C, Dysentery Bacillus 30C, 200C.
For the temporary relief of symptoms related to allergies to Vitamin C in foods and supplements, including fatigue, upper respiratory, gastrointestinal, musculoskeletal, and urinary symptoms.
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use.
Tamper seal: "Sealed for Your Protection."
Do not use if seal is broken or missing.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
3 to 10 drops under the tongue 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
For the temporary relief of symptoms related to allergies to Vitamin C in foods and supplements, including fatigue, upper respiratory, gastrointestinal, musculoskeletal, and urinary symptoms.
Demineralized Water, 25% Ethanol
DESBIO
NDC 43742-0576-1
HOMEOPATHIC
FRUIT ALLERGEN
MIX
1 FL OZ (30 ml)
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACETALDEHYDE | ACTIVE INGREDIENT | GO1N1ZPR3B | 1 | |
| ACETIC ACID | ACTIVE INGREDIENT | Q40Q9N063P | 1 | |
| ADENOSINE TRIPHOSPHATE DISODIUM | ACTIVE INGREDIENT | 5L51B4DR1G | 1 | |
| ARSENIC TRIOXIDE | ACTIVE INGREDIENT | S7V92P67HO | 1 | |
| ASCORBIC ACID | ACTIVE INGREDIENT | PQ6CK8PD0R | 1 | |
| ATROPA BELLADONNA | ACTIVE INGREDIENT | WQZ3G9PF0H | 1 | |
| CINNAMIC ACID | ACTIVE INGREDIENT | U14A832J8D | 1 | |
| CORTICOTROPIN | ACTIVE INGREDIENT | K0U68Q2TXA | 1 | |
| GALLIC ACID MONOHYDRATE | ACTIVE INGREDIENT | 48339473OT | 1 | |
| HESPERIDIN | ACTIVE INGREDIENT | E750O06Y6O | 1 | |
| LACTIC ACID, L- | ACTIVE INGREDIENT | F9S9FFU82N | 1 | |
| MALVIN | ACTIVE INGREDIENT | I9I120531L | 1 | |
| OXALIC ACID DIHYDRATE | ACTIVE INGREDIENT | 0K2L2IJ59O | 1 | |
| QUERCETIN | ACTIVE INGREDIENT | 9IKM0I5T1E | 1 | |
| RUTIN | ACTIVE INGREDIENT | 5G06TVY3R7 | 1 | |
| SHIGELLA DYSENTERIAE | ACTIVE INGREDIENT | 1EP6R5562J | 1 | |
| SODIUM COPPER CHLOROPHYLLIN | ACTIVE INGREDIENT | 1D276TYV9O | 1 | |
| SUS SCROFA ILEUM | ACTIVE INGREDIENT | C998R1XSRA | 1 | |
| SUS SCROFA JEJUNUM | ACTIVE INGREDIENT | TA501QD69R | 1 | |
| SUS SCROFA STOMACH | ACTIVE INGREDIENT | T0920P9Z9A | 1 | |
| ACETALDEHYDE | ACTIVE MOIETY | GO1N1ZPR3B | 1 | |
| ACETIC ACID | ACTIVE MOIETY | Q40Q9N063P | 1 | |
| ADENOSINE TRIPHOSPHATE | ACTIVE MOIETY | 8L70Q75FXE | 1 | |
| ARSENIC CATION (3+) | ACTIVE MOIETY | C96613F5AV | 1 | |
| ASCORBIC ACID | ACTIVE MOIETY | PQ6CK8PD0R | 1 | |
| ATROPA BELLADONNA | ACTIVE MOIETY | WQZ3G9PF0H | 1 | |
| CHLOROPHYLL | ACTIVE MOIETY | 00WNZ48OR9 | 1 | |
| CINNAMIC ACID | ACTIVE MOIETY | U14A832J8D | 1 | |
| CORTICOTROPIN | ACTIVE MOIETY | K0U68Q2TXA | 1 | |
| GALLIC ACID | ACTIVE MOIETY | 632XD903SP | 1 | |
| HESPERIDIN | ACTIVE MOIETY | E750O06Y6O | 1 | |
| LACTIC ACID, L- | ACTIVE MOIETY | F9S9FFU82N | 1 | |
| MALVIN | ACTIVE MOIETY | I9I120531L | 1 | |
| OXALIC ACID | ACTIVE MOIETY | 9E7R5L6H31 | 1 | |
| QUERCETIN | ACTIVE MOIETY | 9IKM0I5T1E | 1 | |
| RUTIN | ACTIVE MOIETY | 5G06TVY3R7 | 1 | |
| SHIGELLA DYSENTERIAE | ACTIVE MOIETY | 1EP6R5562J | 1 | |
| SUS SCROFA ILEUM | ACTIVE MOIETY | C998R1XSRA | 1 | |
| SUS SCROFA JEJUNUM | ACTIVE MOIETY | TA501QD69R | 1 | |
| SUS SCROFA STOMACH | ACTIVE MOIETY | T0920P9Z9A | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 43742-0576 | 43742-0576-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ADENOSINE TRIPHOSPHATE DISODIUM | 5L51B4DR1G | ACTIB |
| ACETALDEHYDE | GO1N1ZPR3B | ACTIB |
| CINNAMIC ACID | U14A832J8D | ACTIB |
| GALLIC ACID MONOHYDRATE | 48339473OT | ACTIB |
| HESPERIDIN | E750O06Y6O | ACTIB |
| MALVIN | I9I120531L | ACTIB |
| QUERCETIN | 9IKM0I5T1E | ACTIB |
| RUTIN | 5G06TVY3R7 | ACTIB |
| SUS SCROFA ILEUM | C998R1XSRA | ACTIB |
| SUS SCROFA JEJUNUM | TA501QD69R | ACTIB |
| SUS SCROFA STOMACH | T0920P9Z9A | ACTIB |
| SODIUM COPPER CHLOROPHYLLIN | 1D276TYV9O | ACTIB |
| ACETIC ACID | Q40Q9N063P | ACTIB |
| ASCORBIC ACID | PQ6CK8PD0R | ACTIB |
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIB |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| OXALIC ACID DIHYDRATE | 0K2L2IJ59O | ACTIB |
| LACTIC ACID, L- | F9S9FFU82N | ACTIB |
| CORTICOTROPIN | K0U68Q2TXA | ACTIB |
| SHIGELLA DYSENTERIAE | 1EP6R5562J | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 33ac584a-f1ff-4b5e-8b2c-1dac84f50761 | 3560f11d-e5fc-4b2f-bb87-6054060414a1 | 2018-12-13 | Warnings | 33ac584a-f1ff-4b5e-8b2c-1dac84f50761 3560f11d-e5fc-4b2f-bb87-6054060414a1 |
Adverse event summaries are temporarily unavailable. Other product information remains available.