Indications & Usage Section
Loss of strength; Difficult concentration; Palpitations; Rapid pulse.
Adrenal
FDA Label NDC 55714-6007
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 Adrenal (NDC 55714-6007). 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 indications & usage section, dosage & administration section, active ingredient section, purpose section, inactive ingredient section, questions section, warnings section, pregnancy section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration Section
Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) as needed or as directed by a health professional.
Active Ingredient Section
Adrenal gland (human)15x
Purpose Section
Loss of strength; Difficult concentration; Palpitations; Rapid pulse
Inactive Ingredient Section
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.
Questions Section
newtonlabs.net - Questions? 1.800.448.7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013
Warnings Section
Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. Consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
Pregnancy Section
If pregnant or breast-feeding, ask a doctor before use.
Otc - Keep Out Of Reach Of Children Section
Keep out of reach of children.
Package Label
-15x-D007-L01.jpg "Adrenal-(human)-15x-D007-L01.jpg")
Package Label (Adrenal (human) 15x D007 L01)
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