MEDI HYDRO DP B TOX AMPOULE

Manufacturer: Inc MBG
Effective date: 2019-01-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:58:21

Label at a glance#

ProductMEDI HYDRO DP B TOX AMPOULE

Active ingredientADENOSINE

Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Open the lid, press the lid to fill the dropper and apply evenly 3-4 drops to the desired parts, gently tap with the fingers to allow it to absorb

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

WARNINGS SECTION

Discontinue use of the product if any of the following symptoms occurred. Consult a dermatologist if the symptoms got worse.
a) If redness, Swelling, Itchiness, Irritation occurred during using.
b) If the above symptoms started to occur when exposed to direct sunlight.
Do not use on skins with wounds, eczema or dermatitis.

Storage instructions
a) Always close the lid after finish using.
b) Store in a safe place away and out of reach of children.
c) Store in a place with not too high or low temperature, keep awayfrom direct sunlight exposure.

OTC - PURPOSE SECTION

Ampoule that provides skin elasticity with active ingredients such as atelocollagen and 3D hyaluronic acid.

INACTIVE INGREDIENT SECTION

water, butylene glycol, hyaluronic acid, etc.

OTC - ACTIVE INGREDIENT SECTION

ADENOSINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ADENOSINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d676a241-be05-4740-b3ee-1a5f2ed422d2	Product name	4	20180615
dd8bd48f-20d6-43c7-b471-3ae872868afa	Product name	3	20180125
d41954ff-bc63-4b2c-aba0-9146707659d7	Product name	2	20151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70694-0010-1	2021-01-29	C162847	48780-1	ba0f9c33-1a93-a910-e053-dadaa90a0b85	80403f3c-4d9b-80a6-e053-2991aa0a9c36

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70694-0010-1	MEDI HYDRO DP B TOX AMPOULE	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70694-0010	MEDI HYDRO DP B TOX AMPOULE (ADENOSINE) LIQUID [INC MBG]	1	Legacy NDC, 1 package rows	20190125_80403f3c-4d9b-80a6-e053-2991aa0a9c36.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

MEDI HYDRO DP B TOX AMPOULE
ADENOSINE
WATER
BUTYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70694-0010	70694-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ADENOSINE	K72T3FS567	ACTIB
BUTYLENE GLYCOL	3XUS85K0RA	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
80403f3c-4d9c-80a6-e053-2991aa0a9c36			80403f3c-4d9b-80a6-e053-2991aa0a9c36	2019-01-24	Warnings	Exact identifier spl id: 80403f3c-4d9c-80a6-e053-2991aa0a9c36 spl set id: 80403f3c-4d9b-80a6-e053-2991aa0a9c36

Reported adverse events (FAERS/openFDA)#

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