Label: CHILDRENS DYE FREE ALLERGY RELIEF- diphenhydramine hcl solution
- NDC Code(s): 11822-0918-1
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 11, 2024
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- 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
FREE
FROM
SUGAR FREE
ALCOHOL FREECompare to the
active ingredient in
Children’s Benadryl®
Dye-Free Allergy*NDC 11822-0918-1
AGES 6-11
CHILDREN’S
DYE-FREE
ALLERGY RELIEFDIPHENHYDRAMINE
HCl 12.5 mg / 5 mL
Oral Solution
ANTIHISTAMINEfor relief of:
sneezing,
runny nose,
itchy throat or nose,
itchy, watery eyesCLEAR BUBBLE
GUM FLAVORDOSAGE CUP INCLUDED
4 FL OZ (118 mL)
*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the registered
trademark Children’s Benadryl® Dye-Free Allergy.50844 ORG012301836
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSINGOUR PROMISE
Dye FreeDOSAGE CUP INCLUDED
DISTRIBUTED BY:
RITE AID
200 NEWBERRY COMMONS
ETTERS, PA 17319
www.riteaid.comSATISFACTION
GUARANTEE
If you’re not satisfied, we’ll
happily refund your money.Rite Aid 44-018
-
INGREDIENTS AND APPEARANCE
CHILDRENS DYE FREE ALLERGY RELIEF
diphenhydramine hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0918 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:11822-0918-1 1 in 1 CARTON 05/01/2023 1 118 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 05/01/2023 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(11822-0918) , pack(11822-0918)