Label: EQUALINE ALLERGY- diphenhydramine hcl solution
- NDC Code(s): 41163-379-26, 41163-379-34
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 24, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)*
- Purpose
- Uses
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Warnings
Do not use
- •
- with any other product containing diphenhydramine, even one used on skin
- •
- to make a child sleepy
Ask a doctor before use if the child has
- •
- a breathing problem such as chronic bronchitis
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- glaucoma
- •
- a sodium-restricted diet
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Directions
- •
- find right dose on chart below
- •
- mL = milliliter
- •
- take every 4 to 6 hours, or as directed by a doctor
- •
- do not take more than 6 doses in 24 hours
Age (yr)
Dose (mL)
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
Attention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
compare to Children’s Benadryl® Allergy Liquid active ingredient
children’s
allergy
diphenhydramine HCl 12.5 mg/5 mL
oral solution (antihistamine)
blocks histamine
relieves:
runny nose
sneezing
itchy, watery eyes
itchy throat
4-6 Hours/Dose
for ages 6 to 11
cherry flavor
ALCOHOL FREE
4 FL OZ (118mL)
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INGREDIENTS AND APPEARANCE
EQUALINE ALLERGY
diphenhydramine hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-379 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) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 40 (UNII: WZB9127XOA) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) POLOXAMER 407 (UNII: TUF2IVW3M2) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color RED (Bluish-Red) Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-379-26 1 in 1 CARTON 08/17/2004 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:41163-379-34 1 in 1 CARTON 08/10/2004 12/25/2011 2 236 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 final part341 08/10/2004 Labeler - United Natural Foods, Inc. dba UNFI (943556183)