Formula 1

Manufacturer
20Lighter, LLC.
Effective date
2021-11-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:15:10

Label at a glance#

ProductFormula 1
Active ingredientADENOSINE TRIPHOSPHATE, LARD, SUS SCROFA CEREBRUM, COENZYME A, SUS SCROFA COLON, SUS SCROFA DUODENUM, BOS TAURUS BILE, FUMARIC ACID, THYROID, PORCINE, PORK LIVER, BOS TAURUS HYPOTHALAMUS, PYRUVALDEHYDE, GLYOXAL, SUS SCROFA PANCREAS
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Equal Amounts of: ATP 30X, Adeps suillus 30C, Adrenal cortex suis 30C, Alpha-ketoglutaricum acidum 30C, Cerebrum suis 30C, Coenzyme A 30X, Colon suis 30X, 60X, 200X, Duodenum suis 30X, 60X, 200X, Fel suis 8X, 12X, Fel tauri 30C, 60C, 200C, Fumaricum acidum 60X, Glandula thyreoidea suis 30C, Hepar suis 30C, Hypothalamus suis 30C, Ileum suis 30X, 60X, 200X, Jejunum suis 30X, 60X, 200X, Malicum acidum 60X, Methylglyoxal 60X, Oxalaldehyde 60X, Pancreas suis 30X, 60X, 200X, Pituitary gland suis 30C, Ventriculus 30X, 60X, 200X.

* Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION

USES: For the temporary relief of symptoms of food cravings, including: constant appetite, increased or insatiable hunger.*

WARNINGS SECTION

WARNINGS:
▀ KEEP OUT OF REACH OF CHILDREN.
▀ IF PREGNANT OR BREAST-FEEDING ask your
doctor before use.
▀ Do not use if you have ever had an allergic
reaction to this product or any of its ingredients.
▀ Stop use if symptoms persist, worsen, or if new
symptoms occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

▀ KEEP OUT OF REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Use as directed by a healthcare professional.

OTHER SAFETY INFORMATION

OTHER INFORMATION: Store at room temperature out of direct sunlight. Tamper resistant for your protection. Do not use if tamper evident seal is missing or broken.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethanol 20%, Purified Water.

OTC - QUESTIONS SECTION

Manufactured for:
20Lighter, LLC
1903 S Greeley Highway, Suite 324
Cheyenne, WY 82007
Tel: (307) 287-1555

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 73399-001-30

20Lighter Program

Formula #1

Homeopathic Remedy

1 fl oz. (30mL)

Ethanol 20%

1 oz bottle label1 oz bottle label

1 oz bottle label1 oz bottle label

OTC - PURPOSE SECTION

For the temporary relief of symptoms of food cravings, including: constant appetite, increased or insatiable hunger.*

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73399-001-302025-01-30C16284748780-12cef2736-9a15-d83d-e063-dadaa90ab31fFormula 1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73399-001-30Formula 130 mL in 1 BOTTLELIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73399-001FORMULA 1 (ATP, ADEPS SUILLUS, ADRENAL CORTEX SUIS, ALPHA KETOGLUTARICUM ACIDUM, CEREBRUM SUIS, COENZYME A, COLON SUIS, DUODENUM SUIS, FEL SUIS, FEL TAURI, FUMARICUM ACIDUM, GLANDULA THYREOIDEA SUIS, HEPAR SUIS, HYPOTHALAMUS SUIS, LLEUM SUIS, JEJUNUM SUIS, MALICUM ACIDUM, METHYLGLYOXAL, OXALALDEHYDE, PANCREAS SUIS, PITUITARY GLAND SUIS, VENTRICULUS) LIQUID [20LIGHTER, LLC.]3Legacy NDC, 1 package rows20211116_8d14b8ca-268e-4db2-86fb-6427ad6bf9f3.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73399-00173399-001-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
8884d1f0-cace-4c1c-86cb-d344962a164e8d14b8ca-268e-4db2-86fb-6427ad6bf9f32021-11-15WarningsExact identifier
spl id: 8884d1f0-cace-4c1c-86cb-d344962a164e
spl set id: 8d14b8ca-268e-4db2-86fb-6427ad6bf9f3

Reported adverse events (FAERS/openFDA)#

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