Formula 2

Manufacturer
20Lighter, LLC.
Effective date
2021-11-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:15:10

Label at a glance#

ProductFormula 2
Active ingredientCHASTE TREE FRUIT, ALPHA LIPOIC ACID, ANDROSTERONE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CINCHONA OFFICINALIS BARK, CYNARA SCOLYMUS LEAF, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, QUERCETIN, LACTIC ACID, L-, SEROTONIN, STRYCHNOS IGNATII SEED, TILIROSIDE, UBIDECARENONE, VALERIAN
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Equal Amounts of: Adipose Tissue Suis 200C, Agnus Castus 60X, Alpha-lipoicum acidum 30X, 60X, 200X, Androsterone (1-DHEA) 30X, Bacopa 30C, Calcarea carbonica 30C, Chlorogenic acids 30C, Cinchona officinalis 30X, 60X, 200X, Cynara Scolymus 60X, Dopamine Hydrochloride 30C, Hydrastis canadensis 30X, 60X, Lycopodium clavatum 30X, Morgan gaertner 30C, Morgan pure 30C, Muscle Suis 200C, Oxytocin acetate 30X, 60X, 200X, Proteus bach 30C, Quercetin 30X, 60X, 200X, Rhodiola 30X, 60X, 200X, Sarcolacticum

* 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

▀ 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.

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

73399-002-30

20Lighter Program

Formula #2

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

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73399-002-30Formula 230 mL in 1 BOTTLELIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73399-002FORMULA 2 (AGNUS CASTUS, ALPHA LIPOICUM ACIDUM, ANDROSTERONE 1 DHEA, CALCAREA CARBONICA,CINCHONA OFFICINALIS, CYNARA SCOLYMUS, DOPAMINE HYDROCHLORIDE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, OXYTOCIN ACETATE, QUERCETIN, SARCOLACTICUM, SEROTONIN, IGNATIA AMARA, TILIROSIDE, UBIQUINONE, VALERIANA OFFICINALIS,) LIQUID [20LIGHTER, LLC.]2Legacy NDC, 1 package rows20211116_9e4caf7f-e1cc-4b24-a78b-71115390bb6a.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73399-00273399-002-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
bb4c2923-7ed8-4e17-a8ae-e0653d1665899e4caf7f-e1cc-4b24-a78b-71115390bb6a2021-11-15WarningsExact identifier
spl id: bb4c2923-7ed8-4e17-a8ae-e0653d166589
spl set id: 9e4caf7f-e1cc-4b24-a78b-71115390bb6a

Reported adverse events (FAERS/openFDA)#

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