2 Transform

Manufacturer
2 Transform | Apotheca Company
Effective date
2021-06-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:41:45

Label at a glance#

Product2 Transform
Active ingredientFUCUS VESICULOSUS, CHELIDONIUM MAJUS, DIBASIC POTASSIUM PHOSPHATE, LYCOPODIUM CLAVATUM SPORE, SODIUM CHLORIDE, QUERCUS ROBUR NUT, QUERCUS ROBUR TWIG BARK, STRYCHNOS NUX-VOMICA SEED, PHYTOLACCA AMERICANA ROOT, ORNITHOGALUM UMBELLATUM, CHASTE TREE FRUIT, BERBERIS AQUIFOLIUM ROOT BARK, BERBERIS VULGARIS ROOT BARK, SUCROSE, SOLIDAGO VIRGAUREA FLOWERING TOP, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACTIVATED CHARCOAL, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SINAPIS ARVENSIS FLOWERING/FRUITING TOP, UBIDECARENONE, GRAPHITE, SUS SCROFA PITUITARY GLAND, SUS SCROFA PLACENTA, BOS TAURUS HYPOTHALAMUS
Label structure9 sections

Dosage and administration

.50ml or 15 drops three times a day. Let rest under the tongue for 60-120 seconds, then swallow. Avoid eating or drinking 15 minutes before and after taking drops. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Fucus Vesiculosus 4X, Chelidonium Majus 6X, Kali Phosphoricum 6X, Lycopodium Clavatum 6X, Natrum Muriaticum 6X, Quercus Glandium Spiritus 6X, Quercus Robur 6X, Nux Vomica 6X, 12X, 30X, Phytolacca Decandra 6X, 12X, 30X, Ornithogalum Umbellatum 8X, Agnus Castus 8X, 12X, 30X, 60X, 200X, Berberis Aquifolium 8X, 12X, 30X, 60X, 200X, Berberis Vulgaris 8X, 12X, 30X, 60X, 200X, Saccharum Officinale 8X, 12X, 30X, 60X, 200X, Solidago Virgaurea 12X, Calcarea Carbonica 12X, Carbo Vegetabilis 12X, Magnesia Phosphorica 12X, Natrum Phosphoricum 12X, Sinapis Arvensis, Flos 12X, Ubidecarenonum 12X, Graphites 12X, 30X, Hypophysis Suis 12X, 30X, 60X, Placenta Totalis Suis 12X, 30X, 60X, Hypothalamus (Bovine) 16X, 30X, 60X.

INDICATIONS:

OTC - PURPOSE SECTION

For diet and inflammation support.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact 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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

.50ml or 15 drops three times a day. Let rest under the tongue for 60-120 seconds, then swallow. Avoid eating or drinking 15 minutes before and after taking drops. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For diet and inflammation support.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Coptis (Root), Demineralized water, Ethanol (20%), L-Arginine, L-Cysteine, L-Leucine, L-Proline, L-Serine, L-Threonine, L-Valine.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by: 2 Transform

170 US Route 1, Suite 110

Falmouth, ME 04105   1-800-540-5906

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2Transform

Homeopathic Drops

Weight Management

Support

2fl.oz. (60 ml)

2Transform2Transform

Products#

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

DailyMed product names page 1 of 2 · 41 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72940-000172940-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
0d579dd1-e3f3-4b24-8fc2-1afc39705db609c42549-cf45-4e05-9b92-b56e3a3768162021-06-29WarningsExact identifier
spl id: 0d579dd1-e3f3-4b24-8fc2-1afc39705db6
spl set id: 09c42549-cf45-4e05-9b92-b56e3a376816

Reported adverse events (FAERS/openFDA)#

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