Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution
- NDC Code(s): 50844-018-36
- Packager: L.N.K. International, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 8, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Uses
- Warnings
-
Directions
- find right dose on chart below
- mL = milliliter; FL OZ = fluid ounce
- use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.
- 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
- find right dose on chart below
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
Quality
PlusNDC 50844-018-36
Compare to active ingredient
in Children’s Benadryl®
Dye-Free Allergy*CHILDREN’S
ALLERGY
RELIEFDiphenhydramine HCl 12.5 mg
AntihistamineRelieves
• Sneezing
• Runny nose
• Itchy, Watery eyes
• Itchy throat
or noseBubble Gum
FlavorALCOHOL FREE • DYE-FREE
SUGAR FREE4 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 ORG121701836
Distributed by
LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788
USATAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSINGQuality Plus 44-018
-
INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY RELIEF
diphenhydramine hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50844-018 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:50844-018-36 1 in 1 CARTON 12/31/2018 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 12/31/2018 Labeler - L.N.K. International, Inc. (038154464) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(50844-018) , pack(50844-018)