BERBERIS AQUARIUS

Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Effective date: 2016-03-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:07:56

Label at a glance#

ProductBERBERIS AQUARIUS

Active ingredientMAHONIA AQUIFOLIUM ROOT BARK

Label structure9 sections

Indications and uses

Acne, blotches, pimples, rough scaly skin, clears the complexion

Storage and handling

Store in a cool dark place

Contacts and useful links#

Websitewww.rxhomeo.com

www.Rxhomeo.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BERBERIS AQUARIUS GEL TINC HPUS

USES

OTC - PURPOSE SECTION

Acne, blotches, pimples, rough scaly skin, clears the complexion

INDICATIONS

INDICATIONS & USAGE SECTION

Condition listed above or as directed by the physician

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer of Gel to the affected area, repeat 3 times a day or as needed.

WARNINGS

WARNINGS SECTION

This product is to be used for self-limiting conditions

OTC - STOP USE SECTION

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

OTC - PREGNANCY OR BREAST FEEDING SECTION

As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children

OTC - DO NOT USE SECTION

Do not use if capseal is broken or missing.
Close the cap tightly after use.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ALOE VERA GEL

STORAGE

STORAGE AND HANDLING SECTION

Store in a cool dark place

QUESTIONS OR COMMENTS

OTC - QUESTIONS SECTION

www.rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
15631-2308-0	2020-01-31	C162847	48780-1	9d75b9d0-40de-f424-e053-dadaa90a57ce	7b97537a-2d33-4ef5-a193-7e7e9559b5b8
15631-2308-1	2020-01-31	C162847	48780-1	9d75b9d0-40de-f424-e053-dadaa90a57ce	7b97537a-2d33-4ef5-a193-7e7e9559b5b8
15631-2308-2	2020-01-31	C162847	48780-1	9d75b9d0-40de-f424-e053-dadaa90a57ce	7b97537a-2d33-4ef5-a193-7e7e9559b5b8
15631-2308-3	2020-01-31	C162847	48780-1	9d75b9d0-40de-f424-e053-dadaa90a57ce	7b97537a-2d33-4ef5-a193-7e7e9559b5b8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
15631-2308-0	BERBERIS AQUARIUS	1 in 1 CONTAINER	GEL	1	1
15631-2308-0	BERBERIS AQUARIUS	50 g in 1 CONTAINER	GEL	50	1
15631-2308-1	BERBERIS AQUARIUS	100 g in 1 CONTAINER	GEL	100	1
15631-2308-1	BERBERIS AQUARIUS	1 in 1 CONTAINER	GEL	1	1
15631-2308-2	BERBERIS AQUARIUS	200 g in 1 CONTAINER	GEL	200	1
15631-2308-2	BERBERIS AQUARIUS	1 in 1 CONTAINER	GEL	1	1
15631-2308-3	BERBERIS AQUARIUS	500 g in 1 CONTAINER	GEL	500	1
15631-2308-3	BERBERIS AQUARIUS	1 in 1 CONTAINER	GEL	1	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
15631-2308	BERBERIS AQUARIUS GEL [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]	1	Legacy NDC, 8 package rows	20160519_7b97537a-2d33-4ef5-a193-7e7e9559b5b8.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

BERBERIS AQUARIUS
MAHONIA AQUIFOLIUM ROOT BARK
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
15631-2308	15631-2308-0, 15631-2308-1, 15631-2308-2, 15631-2308-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAHONIA AQUIFOLIUM ROOT BARK	VZJ9F3C3SB	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT

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
197342e9-995f-4fd0-a83d-6e4d137c496b			7b97537a-2d33-4ef5-a193-7e7e9559b5b8	2016-03-30	Warnings	Exact identifier spl id: 197342e9-995f-4fd0-a83d-6e4d137c496b spl set id: 7b97537a-2d33-4ef5-a193-7e7e9559b5b8

Reported adverse events (FAERS/openFDA)#

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