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
Medi Hydro Dp B Tox Ampoule
FDA Label NDC 70694-0010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Inc Mbg for the product Medi Hydro Dp B Tox Ampoule (NDC 70694-0010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, otc - keep out of reach of children, dosage & administration, warnings, otc - purpose, inactive ingredient, otc - active ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
for external use only
Warnings
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
ADENOSINE
Package Label.Principal Display Panel
Label (Label)
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