NDC | 70694-0010-1 |
Set ID | 80403f3c-4d9b-80a6-e053-2991aa0a9c36 |
Category | HUMAN OTC DRUG LABEL |
Packager | Inc MBG |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
-
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. - PURPOSE
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MEDI HYDRO DP B TOX AMPOULE
adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70694-0010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70694-0010-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/24/2019 Labeler - Inc MBG (688436167) Establishment Name Address ID/FEI Business Operations Inc MBG 688436167 manufacture(70694-0010)