Dhea
FDA Label NDC 63776-653

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Viatrexx Bio Incorporated for the product Dhea (NDC 63776-653). 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 active ingredients, purpose:, uses, warnings, dosage, other ingredients, other information, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Dehydroepiandrosterone 6X, 200K

Purpose:

DehydroepiandrosteroneHormone support

Uses

To help with symptoms of low sex drive & low immune system

Warnings

Stop use and ask a health care practitioner if symptoms persist for more than five days or worsen. If pregnant or breastfeeding, ask a health care practitioner before use.

Dosage

1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Other Ingredients

20% Alcohol and 80% Water

Other Information

Normal storage use.

Do not use if tamper-evident seal is broken or removed.

Principal Display Panel

ITEM: VP0055

NDC 63776-653-14

Homeopathic remedy

DHEA

To help with symptoms of low sex drive & low immune system

Oral spray
30ml 1 oz

Viatrexx™ Bio Incorporated

Manufactured by Viatrexx
www.viatrexx.com
Newark, DE 19713

Dhea Carton (Dhea B)

Dhea Carton (Dhea B)

DHEA

30 ml
1 oz

Viatrexx™ Bio Incorporated

ITEM: VP0055
NDC: 63776-653-14

INDICATIONS:
To help with symptoms of low sex drive & low immune system

DIRECTIONS:
1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Mfg. for
Viatrexx Bio Incorporated.
www.viatrexx.com
Newark, DE 19713

Ingredients (Dhea L)

Ingredients (Dhea L)

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