D-79- urtica urens, toxicodendron pubescens leaf, and echinacea angustifolia 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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D-79

NDC 58264-0080-1

INDICATIONS

Allergy to poison oak or ivy.

INGREDIENTS

ACTIVE

Urtica urens 3x, Rhus toxicodendron 3x, Echinacea angustifolia 2x

INACTIVE

20% alcohol in purified water.

SUGGESTED DOSAGE

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

SHAKE WELL

Warnings

  • 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.

D 79

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
D-79 
urtica urens, toxicodendron pubescens leaf, and echinacea angustifolia solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0080
Route of AdministrationSUBLINGUAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS3 [hp_X]  in 1 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF3 [hp_X]  in 1 mL
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA2 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58264-0080-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/01/1990
Labeler - DNA Labs, Inc. (031784339)

Revised: 6/2022
Document Id: e0bae390-0bd9-159f-e053-2a95a90ac095
Set id: 0dd8244d-4cd4-4fa8-980a-6089278824dc
Version: 2
Effective Time: 20220605
 
DNA Labs, Inc.