HEB ANTI NAUSEA (dextrose(glucose),levulose- fructose,phosphoric acid liquid

HEB Anti Nausea by

Drug Labeling and Warnings

HEB Anti Nausea by is a Otc medication manufactured, distributed, or labeled by HEB. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (per 5 mL)

Dextrose (glucose) 1.87 g

Levulose (fructose) 1.87 g

•   Phosphoric acid 21.5 mg

Purpose

Upset Stomach Reliever

Uses

• ▪ for relief of upset stomach associated with nausea

Warnings

• ▪ this product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI).

Do not use if you have

• ▪ allergic reactions to any of the ingredients in this product

Ask a doctor before use if you have

• ▪ diabetes

Stop use and ask a doctor if

• ▪ symptoms persist, return or get worse

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away at (1-800-222-1222)

Directions

• ▪ for maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product
• ▪ repeat dose every 15 minutes or until distress subsides
• ▪ do not take more than 5 doses in 1 hour without consulting a doctor
• ▪ measure only with dosing cup provided. Dosing cup to be used with this product only. Do not use with other products.
• ▪ mL= milliliter

• age:
  • dose
• adults and children 12 years of age and over:
  • 15 mL or 30 mL
• children 2 to under 12 years of age:
  • 5 ml or 10 mL

Other information

• store at room temperature away from heat and direct light; keep from freezing
• do not use if printed seal under cap is broken or missing

Inactive ingredients

FD&C Red No. 40, flavors, glycerin, methylparaben, purified water.

Questions or Comments?

1-866-467-2748

SPL UNCLASSIFIED SECTION

NDC: 37808-883-04

Compare to the active ingredients Emetrol®*

Anti-Nausea Liquid

Relief from nausea due to upset stomach Safe and effective for children and adults

• No antihistamines
• No salicylates
• No caffeine

Cherry Flavor

Naturally and Artificially Flavored

4 FL OZ (118 mL)

IMPORTANT: Keep this carton for future reference on full labeling.

*This product is not manufactured or distributed by Wellspring Pharmaceutical Corporation., owner of the registered trademark Emetrol®.

PACKAGE LABEL

 

INGREDIENTS AND APPEARANCE

HEB ANTI NAUSEA 
dextrose(glucose),levulose(fructose),phosphoric acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-883
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) (DEXTROSE, UNSPECIFIED FORM - UNII:IY9XDZ35W2)	DEXTROSE, UNSPECIFIED FORM	1.87 g  in 5 mL
FRUCTOSE (UNII: 6YSS42VSEV) (FRUCTOSE - UNII:6YSS42VSEV)	FRUCTOSE	1.87 g  in 5 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	21.5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	RED (Red)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-883-04	1 in 1 CARTON	04/20/2020
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		04/20/2020

Labeler - HEB (007924756)