NDC 70694-0010 Medi Hydro Dp B Tox Ampoule


NDC Product Code 70694-0010

NDC Product Information

Medi Hydro Dp B Tox Ampoule with NDC 70694-0010 is a a human over the counter drug product labeled by Inc Mbg. The generic name of Medi Hydro Dp B Tox Ampoule is adenosine. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Inc Mbg

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Medi Hydro Dp B Tox Ampoule Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ADENOSINE .04 g/100mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

Additional informationCallout TooltipWhat are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Medi Hydro Dp B Tox Ampoule Product Label Images

Medi Hydro Dp B Tox Ampoule Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

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

Keep out of reach of children.

Dosage & Administration

For external use only


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

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

Inactive Ingredient

Water, butylene glycol, hyaluronic acid, etc.

Otc - Active Ingredient


* Please review the disclaimer below.

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