Label: INTOMEDI AMPLANCE HYDRO- adenosine liquid
- NDC Code(s): 82879-0001-1
- Packager: Janytree Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 12, 2022
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- Official Label (Printer Friendly)
- INACTIVE INGREDIENTS
- ACTIVE INGREDIENTS
- PURPOSE
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WARNINGS
For external use only When using this product
■ If following abnormal symptoms occurs after using the product, stop using the product and consult with a skin specialist. Symptoms : Red specks, swelling, itching
■ Do not use on the skin parts affected by wound, eczema, or dermatitis.
Keep out of reach of children.
■ If swallowed, get a medical help or contact a person in control center immediately.
■ Avoid contact with eyes. - KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INTOMEDI AMPLANCE HYDRO
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82879-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82879-0001-1 50 g in 1 TUBE; Type 0: Not a Combination Product 07/13/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/13/2022 Labeler - Janytree Inc. (688403840) Registrant - Janytree Inc. (688403840) Establishment Name Address ID/FEI Business Operations Janytree Inc. 688403840 manufacture(82879-0001)