Morningcalm V Zero

Manufacturer: Morningcalmsalt Co., Ltd.
Effective date: 2020-08-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:24:17

Label at a glance#

ProductMorningcalm V Zero

Active ingredientZEOLITE A

Label structure8 sections

Dosage and administration

for external use only

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

zeolite

Purpose

OTC - PURPOSE SECTION

Anti-virus mineral deodorant

Use

INDICATIONS & USAGE SECTION

Spray Morningcalm V Zero at the place used as
high as possible for maximum effect (it is effective
to allow more than 1 second of time to pass ).
• Spray Morningcalm V Zero on object (mask, clothes,
shoes, etc.) and dry it to increase the effect

Warnings

WARNINGS SECTION

Do not use Morningcalm V Zero for any purpose other
than deodorant. If Morningcalm V Zero is sprayed
in your face or eyes, wash them with cold water
immediately.
• Do not spill Morningcalm V Zero excessively on
one spot as it may cause slipperiness.
• Do not use Morningcalm V Zero in areas
at risk of discoloration or
bleaching.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Bentonite, Sericite, Sulfur, Molybdate , Calcium , Chitosan, Iodine, Purified water, etc.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78811-0001-1	2022-01-28	C162847	48780-1	d6a99b39-e925-a426-e053-dadaa90af4c2	aa273c2b-ca8f-4407-e053-2a95a90acc07

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78811-0001-1	Morningcalm V Zero	500 mL in 1 BOTTLE	LIQUID	500		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78811-0001	MORNINGCALM V ZERO (ZEOLITE) LIQUID [MORNINGCALMSALT CO., LTD.]	2	Legacy NDC, 1 package rows	20200811_aa273c2b-ca8f-4407-e053-2a95a90acc07.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Morningcalm V Zero
Zeolite
CALCIUM
SODIUM MOLYBDATE DIHYDRATE
GLYCERIN
WATER
ZEOLITE A
POTASSIUM IODIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78811-0001	78811-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CALCIUM	SY7Q814VUP	IACT
SODIUM MOLYBDATE DIHYDRATE	8F2SXI1704	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ZEOLITE A	Y3NG9WF08W	ACTIB
POTASSIUM IODIDE	1C4QK22F9J	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
ac9011d1-e2c0-4684-e053-2995a90af63c			aa273c2b-ca8f-4407-e053-2a95a90acc07	2020-08-10	Warnings	Exact identifier spl id: ac9011d1-e2c0-4684-e053-2995a90af63c spl set id: aa273c2b-ca8f-4407-e053-2a95a90acc07

Reported adverse events (FAERS/openFDA)#

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