Other
NDC 58264-0301-1
To be used according to standard homeopathic indications.
A-9 Solution
FDA Label NDC 58264-0301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dna Labs, Inc. for the product A-9 (NDC 58264-0301). 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 other, otc - purpose, inactive ingredient, suggested dosage, warnings, otc - pregnancy or breast feeding, otc - keep out of reach of children, principal display panel - 1 fl. oz. bottle label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Allergies.
Inactive Ingredient
House dust 6/12/30x, Mattress dust 6/12/30x, Upholstery dust 6/12/30x, Rug dust 6/12/30x, 20% alcohol in purified water.
Suggested Dosage
Normal dose for the first week is 2-3 drops in water T.I.D. Add one drop per dose per week until a total of ten drops is reached.
SHAKE WELL
Warnings
- Use only if cap seal is unbroken.
Otc - Pregnancy Or Breast Feeding
- As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.
Otc - Keep Out Of Reach Of Children
- Keep this and all medication out of the reach of children.
Principal Display Panel - 1 Fl. Oz. Bottle Label
DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.
A-9
DUST MIX
HOMEOPATHIC ANTIGEN
1 FL. OZ.
Principal Display Panel (1 FL. OZ. Bottle Label)
* Please review the disclaimer below.
