A-26- artemisia ludoviciana pollen and artemisia tridentata pollen solution
DNA Labs, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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A-26

NDC 58264-0318-1

INDICATIONS

Allergies.

INGREDIENTS

ACTIVE

Prairie 6/12/30x, Common 6/12/30x

INACTIVE

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.

If pregnant or breastfeeding, ask a healthcare professional before use.

Keep this and all medication out of the reach of children.

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

A-26
SAGE MIX

HOMEOPATHIC ANTIGEN

1 FL. OZ.

A-26
artemisia ludoviciana pollen and artemisia tridentata pollen solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58264-0318
Route of Administration	SUBLINGUAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H) (ARTEMISIA LUDOVICIANA POLLEN - UNII:57KIJ4772H)	ARTEMISIA LUDOVICIANA POLLEN	30 [hp_X] in 1 mL
ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD)	ARTEMISIA TRIDENTATA POLLEN	30 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:58264-0318-1	29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/1990

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		01/01/1990

Labeler - DNA Labs, Inc. (031784339)