Attention Plus

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2022-05-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:00:36

Label at a glance#

ProductAttention Plus
Active ingredientARNICA MONTANA, MILK THISTLE, SUS SCROFA CEREBRUM, CINCHONA OFFICINALIS BARK, GINKGO, LECITHIN, SOYBEAN, ACHILLEA MILLEFOLIUM, PHOSPHORIC ACID
Label structure9 sections

Dosage and administration

Adults and children over 12: Spray twice under the tongue 3 times per day. Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 3X, Carduus Marianus 3X, Cerebrum Suis 6X, Cinchona Officinalis 6X, Ginkgo Biloba 6X, Lecithin 12X, Millefolium 3X, Phosphoricum Acidum 30C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with attention disorders: distractibility, lack of attention, poor concentration, emotional fluctuations.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If symptoms persist, consult a doctor.

If pregnant or breast feeding, ask a doctor before use.

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

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray twice under the tongue 3 times per day.

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with attention disorders: distractibility, lack of attention, poor concentration, emotional fluctuations.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY LIDDELL LABORATORIES INC.
WOODBINE, IA 51579
WWW.LIDDELL.NET   1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL

LABORATORIES

EST 1994

17Atn+

Attention Plus

HOMEOPATHIC

1.0 FL OZ. (30 ml)

Attention Plus lblAttention Plus lbl

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0230-12022-05-24C16284748780-19d75b9d0-e33e-f424-e053-dadaa90a57ceDrug Facts:
50845-0230-12022-01-28C16284748780-19d75b9d0-e33e-f424-e053-dadaa90a57ceDrug Facts:
50845-0230-12020-10-22C16284748780-19d75b9d0-e33e-f424-e053-dadaa90a57ceDrug Facts:
50845-0230-12020-01-31C16284748780-19d75b9d0-e33e-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-023050845-0230-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
da53da9d-f25f-4c13-8683-87fa3b745451c43e73da-69cc-4c0e-9557-3f5bc3f59c9c2022-05-24WarningsExact identifier
spl id: da53da9d-f25f-4c13-8683-87fa3b745451
spl set id: c43e73da-69cc-4c0e-9557-3f5bc3f59c9c

Reported adverse events (FAERS/openFDA)#

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