SCHUESSLER TISSUE SALTS COMB D SKIN DISORDERS- kali muriaticum,kali sulphuricum,calcarea sulphurica,silicea spray

Schuessler Tissue Salts Comb D Skin Disorders by

Drug Labeling and Warnings

Schuessler Tissue Salts Comb D Skin Disorders by is a Homeopathic medication manufactured, distributed, or labeled by Martin & Pleasance Pty Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (in each spray)                                      Purpose  

 Calcarea Sulphurica 6X HPUS ............................................ skin disorders, acne
Kali Muriaticum 6X HPUS ................................................... minor skin eruptions
Kali Sulphuricum 6X HPUS ............... dry, scaly & flaky skin, minor skin eruptions
Silicea 6X HPUS .......................................... skin disorders, minor skin eruptions

"HPUS" is the Homeopathic Pharmacopoeia of the United States

PURPOSE

Uses

Temporarily relieves symptoms associated with:

• Skin disorders
• Minor skin eruptions
• Acne
• Dry, scaly & flaky skin

Warnings

Slop use and ask a doctor if:

Symptoms persist for more than 7 days or worsen

Inflammation, fever, or infection is present or develops

Fever gets worse or lasts more than 3 days

If skin eruptions are severe or painful, seek the advice of a doctor.

If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Directions

• Use as directed 
• Take 30 minutes away from food.

Adults

• Acute dose: Spray into the mouth 4 times every 30 mins until symptoms subside, up to 8 times per day.
• Maintenance dose: Spray into mouth 4 times, 4 times per day.

Other Information

Store below 86°F

Inactive Ingredients

Alcohol, Glycerin, Purified Water

SPL UNCLASSIFIED SECTION

Questions?www.schuesslertissuesalts.co or + 1-888-464-6775

Product label

INGREDIENTS AND APPEARANCE

SCHUESSLER TISSUE SALTS COMB D SKIN DISORDERS 
kali muriaticum,kali sulphuricum,calcarea sulphurica,silicea spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84999-028
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	6 [hp_X]  in 30 mL
POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM SULFATE	6 [hp_X]  in 30 mL
CALCIUM SULFATE DIHYDRATE (UNII: 4846Q921YM) (PHOSPHATE ION - UNII:NK08V8K8HR)	CALCIUM SULFATE DIHYDRATE	6 [hp_X]  in 30 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SAND - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84999-028-01	1 in 1 CARTON	08/01/2025
1		30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/01/2025

Labeler - Martin & Pleasance Pty Ltd (752869859)