Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution
- NDC Code(s): 69842-719-19
- Packager: CVS PHARMACY
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 21, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Uses
- Warnings
-
Directions
- do not take more than directed
- find right dose on chart below
- mL = milliliter
- only use the dose cup provided
- 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 doctorchildren 6 to 11 years 5 mL to 10 mL
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
♥CVS
Health®Compare to the active
ingredient in Children’s
Benadryl® Allergy*Dye Free Liquid
Children’s
Allergy
ReliefLIQUID MEDICATION
DIPHENHYDRAMINE HCl
12.5 mg per 5 mL
ORAL SOLUTION
AntihistamineDYE
FREERelief of:
• Sneezing
• Runny nose
• Itchy, watery eyes
• Itchy throatCherry Flavored
Sugar & Alcohol Free
Ages 6 to 11 Years
Actual Bottle Size on Side Panel8 FL OZ (237 mL)
Package Contains
One BottleActual Size
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2023 CVS/pharmacy
CVS.com® 1-800-SHOP CVS
V-18615CVS® Quality
Money Back GuaranteeTAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING*This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of the
registered trademark Children’s Benadryl® Allergy.
50844 REV0123B01719
CVS 44-017
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INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY RELIEF
diphenhydramine hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-719 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 CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-719-19 1 in 1 CARTON 08/05/2020 1 237 mL in 1 BOTTLE, PLASTIC; 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 08/05/2020 Labeler - CVS PHARMACY (062312574) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(69842-719) , pack(69842-719)