Label: ACTIDOSE AQUA- activated charcoal suspension
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NDC Code(s):
0574-0521-04,
0574-0521-08,
0574-0521-25,
0574-0521-74, view more0574-0521-76
- Packager: Padagis US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 1, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient (in each tube)
- Purpose
- Uses
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Warnings
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- Do not give activated charcoal until after the patient has vomited unless directed by a health professional.
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- Do not use in persons who are not fully conscious.
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- Do not use this product, unless directed by a health professional, if turpentine, corrosives (such as alkalies (lye) and strong acids), or petroleum distillates (such as kerosene, gasoline, paint thinner, cleaning fluid, or furniture polish), have been ingested.
- Keep out of reach of children.
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Directions
- Oral Dosage: 20 to 30 grams of activated charcoal in a minimum of 8 ounces of liquid or as directed by a health professional. Repeat dose immediately, if possible.
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- Shake well
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- Snip tapered tip as indicated in drawing and remove. Holding the tube upright, carefully but off tube closure. Reattach tapered tip and connect to any charcoal administration set or squeeze contents in a cup with a minimum of 4 ounces of liquid for patient to drink.
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- If previous attempts to contact a poison control center, emergency medical facility, or health professional were unsuccessful, continue trying.
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- Keep patient active and moving.
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- Save the container of poison.
- Other information
- Inactive Ingredients
- Questions?
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Package/Label Principal Display Panel
NDC 0574-0521-74
ACTIDOSE®-Aqua
ACTIVATED CHARCOAL SUSPENSION
25 grams Activated Charcoal
POISON ADSORBENT
If possible call a Poison Control Center, emergency medical facility, or health professional for help before using this product. If help cannot be reached quickly, follow directions on this label. Read label warnings and directions upon buying this product. Insert emergency phone number(s) in space provided on the label.
Emergency Phone Number:
WARNING: Cancer and Reproductive Harm – www.P65Warnings.ca.gov.
CONTENTS: 120 mL (4 fl oz)
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INGREDIENTS AND APPEARANCE
ACTIDOSE AQUA
activated charcoal suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0574-0521 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 208 mg in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SUCROSE (UNII: C151H8M554) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0574-0521-04 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/11/2020 2 NDC:0574-0521-08 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/11/2020 3 NDC:0574-0521-25 72 mL in 1 TUBE; Type 0: Not a Combination Product 01/31/2023 4 NDC:0574-0521-74 120 mL in 1 TUBE; Type 0: Not a Combination Product 11/10/2020 5 NDC:0574-0521-76 240 mL in 1 TUBE; Type 0: Not a Combination Product 12/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M023 11/10/2020 Labeler - Padagis US LLC (967694121)
