D-68: Homeopathic Product Information

D-68- croton oil, daphne mezereum bark, sodium chloride and toxicodendron pubescens leaf 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.

NDC 58264-0068-1

INDICATIONS

Pustular eruptions.

INGREDIENTS

ACTIVE

Croton tiglium 6x, Merezeum 3x, Natrum muriaticum 6x, Rhus toxicodendron 4x

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

  • 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.

D 68

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

Principal Display Panel -- 1 FL. OZ. Bottle Label
(click image for full-size original)
D-68
croton oil, daphne mezereum bark, sodium chloride, and toxicodendron pubescens leaf solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0068
Route of Administration SUBLINGUAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CROTON OIL (CROTON OIL) CROTON OIL 6 [hp_X] in 1 mL
DAPHNE MEZEREUM BARK (DAPHNE MEZEREUM BARK) DAPHNE MEZEREUM BARK 3 [hp_X] in 1 mL
SODIUM CHLORIDE (CHLORIDE ION and SODIUM CATION) SODIUM CHLORIDE 6 [hp_X] in 1 mL
TOXICODENDRON PUBESCENS LEAF (TOXICODENDRON PUBESCENS LEAF) TOXICODENDRON PUBESCENS LEAF 4 [hp_X] in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:58264-0068-1 29.57 mL in 1 BOTTLE, GLASS None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/01/1990
Labeler — DNA Labs, Inc. (031784339)

Revised: 06/2022 DNA Labs, Inc.

HomeoLabels.com provides trustworthy package insert and label information about marketed homeopathic remedies as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by HomeoLabels.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

We source our database directly from the FDA's central repository of homeopathic remedy labels and package inserts, under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.