Label: CHILDRENS ALLERGY RELIEF liquid
- NDC Code(s): 69168-471-59
- Packager: Allegiant Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 6, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient(s)
- Purpose
- Use(s)
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Warnings
Do not use
- to make a child sleepy
- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if
- a breathing problem such as chronic bronchitis
- glaucoma
- a sodium-restricted diet
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Directions
- do not take more than directed
- do not take more than 6 doses in 24 hours
- mL = milliliter
- only use the dosing cup provided
- find right dose on chart below
- take every 4 to 6 hours, or as directed by a doctor
- children under 2 years: do not use
- children 2 to 5 years: do not use unless directed by a doctor
children 6 to 11 years: 5 mL to 10 mL
- Other information
- Inactive ingredients
- Questions/Comments
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY RELIEF
childrens allergy relief liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69168-471 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 12.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor BUBBLE GUM Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69168-471-59 1 in 1 CARTON 01/07/2025 1 237 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 OTC Monograph Drug M012 01/07/2025 Labeler - Allegiant Health (079501930)