Cold Hands - Feet Liquid
FDA Label NDC 55714-2404

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Newton Laboratories, Inc. for the product Cold Hands - Feet (NDC 55714-2404). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding warnings section, otc - keep out of reach of children section, dosage & administration section, otc - active ingredient section, otc - purpose section, inactive ingredient section, questions section, indications & usage section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warnings Section

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

Dosage & Administration Section

Adults, take 6 drops by mouth one to four times daily or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Otc - Active Ingredient Section

Equal parts of Echinacea 6x, Aconitum nap. 15x, Arsenicum alb. 15x, Bryonia 15x, Cactus 15, Calc. fluor. 15x, Ceanothus 15x, Cinchona 15x, Convallaria 15x, Digitalis 15x, Gelsemium 15x, Glonoinum 15x, Histaminum hydrochloricum 15x, Hydrocotyle 15x, Kali carb. 15x, Lachesis 15x, Naja 15x, Nat. carb. 15x, Nat. mur. 15x, Nux vom. 15x, Phos. 15x, Pulsatilla 15x, Rhus tox. 15x, Strophanthus hisp. 15x, Sulphur 15x, Thyroidinum 15x.

Otc - Purpose Section

Formulated for associated symptoms such as dizziness, fatigue, weakness, tingling and numb or cold extremities.

Inactive Ingredient Section

USP Purified water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

Questions Section

newtonlabs.net - Questions? 800 448-7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

Indications & Usage Section

Formulated for associated symptoms such as dizziness, fatigue, weakness, tingling and numb or cold extremities.

Otc - Pregnancy Or Breast Feeding Section

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

Package Label

Package Label (N052 L01)

Package Label (N052 L01)

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