Label: INSTA-CHAR AQUEOUS- poison treatment adsorbent suspension
- NDC Code(s): 66689-114-08
- Packager: VistaPharm, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 6, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (per 240 mL)
- Purpose
- Uses
-
Warnings
Do not give
- activated charcoal until after patient has vomited unless directed by a health professional
- Do not use in persons who are not fully conscious
- Do not use this product unless directed by a health professional if turpentine, corrosive such as alkalies (lye) and strong acids or petroleum distillates, such as keosene, gasoline, paint thinner, cleaning fluid or furniture polish have been ingested.
-
Directions
- Shake vigorously to suspend charcoal before use.
- remove foil seal underneath cap and replace cap.
- cut off delivery tip of bottle 3/4 inch from end to insert drinking straw included with bottle.
- pull or cut off tip from included cherry flavor and squeeze flavor into straw
- administer entire bottle, 25 g of activated charcoal in 240 mL, or as directed by a health professional.
- repeat dose immediately if possible.
- if previous attempts to contact a poison control center. emergency medical facility, of health professional were unsuccessful, continue trying.
- keep patient active and moving.
- Save the container of poison.
- Other information
- Suspension inactive Ingredients
- Questions?
- Insta-Char Aqueous 240 mL
- Principal Display Panel
- Principal Display Panel -Carton
-
INGREDIENTS AND APPEARANCE
INSTA-CHAR AQUEOUS
poison treatment adsorbent suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66689-114 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 25 g in 240 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) FD&C RED NO. 40 (UNII: WZB9127XOA) SODIUM BENZOATE (UNII: OJ245FE5EU) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66689-114-08 240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 12/13/2024 Labeler - VistaPharm, LLC (048458728)