SUBTILIS DROPS 6X

Manufacturer: USPharmaCo | DermaMed
Effective date: 2009-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:05

Label at a glance#

ProductSubtilis

Active ingredientBacillus subtilis

Label structure10 sections

Storage and handling

Protect from light and heat.

Contacts and useful links#

PhoneLabel contact1-623-582-3110

Websitewww.uspharmaco.com

www.uspharmaco.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Homeopathic Medicine

Indications

INDICATIONS & USAGE SECTION

For temporary relief of constipation, mild cramping, bloating and gas

Dosage

DOSAGE & ADMINISTRATION SECTION

5 drops, three times per week.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Bacillus subtilis 6X

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water, sodium chloride, potassium sorbate.

Warning

WARNINGS SECTION

If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing, seek the advice of a health care professional before using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

STORAGE AND HANDLING SECTION

Protect from light and heat.

Tamper Evident

OTC - DO NOT USE SECTION

Do not use product if the tamper evident strip is broken or removed from the base of the cap.

SPL UNCLASSIFIED SECTION

To report serious adverse events, call: 1-623-582-3110

Manufactured for and distributed by:
USPharmaCo Distribution Ltd.
2205 W. Lone Cactus Drive #19, Phoenix, AZ 85027
www.uspharmaco.com
info@uspharmaco.com

Made in Canada

PRINCIPAL DISPLAY PANEL - 5 mL Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUBTILIS DROPS 6X

Homeopathic Medicine 0.17 fl. oz. (5ml)

Indications: For temporary relief of constipation, mild cramping, bloating and gas
Dosage: 5 drops, three times per week.
Active Ingredient: Bacillus subtilis 6X
Inactive Ingredients: Purified water, sodium chloride, potassium sorbate.
Warning: If symptoms persist more than a few days, contact a licensed practitioner. As with any
drug, if you are pregnant or nursing, seek the advice of a health care professional before using this
product. Keep this and all medications out of reach of children. In case of overdose, get medical help
or contact a Poison Control Center right away. Protect from light and heat.
Tamper Evident: Do not use product if the tamper evident strip is broken or removed from the base
of the cap.
To report serious adverse events, call: 1-623-582-3110

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49693-2301-1	2019-10-21	C162847	48780-1	956f9ecf-c774-621f-e053-dbdaa90a74ad	SUBTILIS DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49693-2301-1	Subtilis	5 mL in 1 BOTTLE	LIQUID	5		1
49693-2301-1	Subtilis	1 in 1 BOX	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49693-2301	SUBTILIS (BACILLUS SUBTILIS) LIQUID [USPHARMACO]	1	Legacy NDC, 2 package rows	20091223_21dc6b8a-f8ec-4073-a8b0-77af0d58fb88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Bacillus subtilis	ACTIVE INGREDIENT	8CF93KW41W	1
Bacillus subtilis	ACTIVE MOIETY	8CF93KW41W	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

Subtilis
Bacillus subtilis

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49693-2301	49693-2301-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Bacillus subtilis	8CF93KW41W	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1b295707-cae6-4a8d-9d90-da81a54e3ab7			21dc6b8a-f8ec-4073-a8b0-77af0d58fb88	2009-12-18	Warnings	Exact identifier spl id: 1b295707-cae6-4a8d-9d90-da81a54e3ab7 spl set id: 21dc6b8a-f8ec-4073-a8b0-77af0d58fb88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.