FDA.reportPublic FDA data

Acidil

Manufacturer
Laboratoires Boiron | Boiron Inc. | Boiron
Effective date
2023-05-09
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 02:21:08

Label at a glance#

ProductAcidil
Active ingredientPICEA MARIANA RESIN, ACTIVATED CHARCOAL, STRYCHNOS NUX-VOMICA SEED, ROBINIA PSEUDOACACIA BARK
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients** (in each tablet)

Abies nigra 4C HPUS (0.63 mg)

Carbo vegetabilis 4C HPUS (0.63 mg)

Nux vomica 4C HPUS (0.63 mg) (contains less than 10 -9 mg strychnine alkaloids)

Robinia pseudoacacia 4C HPUS (0.63 mg)

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Abies nigra 4C HPUS (0.63 mg)..................................................Relieves stomach pain after eating
Carbo vegetabilis 4C HPUS (0.63 mg).......................................Relieves stomach bloating with gas
Nux vomica 4C HPUS (0.63 mg)................. Relieves heartburn due to excessive eating and drinking
Robinia pseudoacacia 4C HPUS (0.63 mg)........................Relieves heartburn with acid indigestion

INDICATIONS & USAGE SECTION

Uses*

Temporarily relieves:

  • heartburn
  • acid indigestion
  • bloating
  • upset stomach associated with these symptoms

WARNINGS SECTION

Warnings

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor ifsymptoms persist for more than 7 days or worsen. If you have trouble swallowing or persistent abdominal pain, see your doctor promptly.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years of age and older: At the onset of symptoms, dissolve 2 tablets in the mouth every 15 minutes for 1 hour until symptoms are relieved. If necessary, dissolve 2 tablets under the tongue15 minutes before meals.


Children under 12 years of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

Croscarmellose sodium, lactose, magnesium stearate

SPL UNCLASSIFIED SECTION

do not use if glue carton flaps are open or if the blister seal is broken

store below 86°F (30°C)

Heartburn relief*

Acid Indigestion Upset Stomach*

No Known Drug Interactions

120 Meltaway Tablets unflavored

60 Meltaway Tablets unflavored

20 Meltaway Tablets unflavored

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

OTC - QUESTIONS SECTION

Questions or comments?

BoironUSA.com
Info@Boiron.com
1-800-BOIRON-1
(1-800-264-7661)

Made in France
Distributed by Boiron Inc.
Newtown Square, PA 19073

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabelslabelslabellabellabellabelLAbelLAbellabellabel689875 10.2019689875 10.2019acidilacidilAcidil Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9004-042023-05-09C16284748780-1f386c649-eab9-0266-e053-dadaa90a7c1aACIDIL
0220-9004-912023-05-09C16284748780-1f386c649-eab9-0266-e053-dadaa90a7c1aACIDIL
0220-9004-042023-01-30C16284748780-1f386c649-eab9-0266-e053-dadaa90a7c1aACIDIL
0220-9004-912023-01-30C16284748780-1f386c649-eab9-0266-e053-dadaa90a7c1aACIDIL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9004-04Acidil60 in 1 BLISTER PACKTABLET6010
0220-9004-29Acidil120 in 1 BLISTER PACKTABLET12010
0220-9004-91Acidil20 in 1 BLISTER PACKTABLET2010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9004ACIDIL (PICEA MARIANA RESIN, ACTIVATED CHARCOAL, STRYCHNOS NUX-VOMICA SEED, ROBINIA PSEUDOACACIA BARK) TABLET [LABORATOIRES BOIRON]10Current NDC, Legacy NDC, 3 package rows20230510_495ad600-7fca-4104-bf7a-4858f946c5e4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H103
PICEA MARIANA RESINACTIVE INGREDIENT71AOV0W1313
ROBINIA PSEUDOACACIA BARKACTIVE INGREDIENT7TPC058OWY3
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139193
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H103
PICEA MARIANA RESINACTIVE MOIETY71AOV0W1313
ROBINIA PSEUDOACACIA BARKACTIVE MOIETY7TPC058OWY3
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139193
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH483
LactoseINACTIVE INGREDIENTJ2B2A4N98G3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I303

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-90040220-9004-04, 0220-9004-91, 0220-9004-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CROSCARMELLOSE SODIUMM28OL1HH48IACT
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
PICEA MARIANA RESIN71AOV0W131ACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
ROBINIA PSEUDOACACIA BARK7TPC058OWYACTIB

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 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LactoseLACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LactoseLACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LactoseLACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
LactoseLACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
4 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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcidilPICEA MARIANA RESIN, ACTIVATED CHARCOAL, STRYCHNOS NUX-VOMICA SEED, ROBINIA PSEUDOACACIA BARKLaboratoires Boiron495ad600-7fca-4104-bf7a-4858f946c5e42023-05-09WarningsExact identifier
ndc (package): 0220-9004-04
ndc (package): 0220-9004-91
ndc (package): 0220-9004-29
ndc (product): 0220-9004
ndc11 (package): 00220900404
ndc11 (package): 00220900491
ndc11 (package): 00220900429
spl id: fb46dcaf-ef71-4f45-e053-6294a90a7a98
spl set id: 495ad600-7fca-4104-bf7a-4858f946c5e4

Reported adverse events (FAERS/openFDA)#

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