Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
- NDC Code(s): 50844-932-08, 50844-932-12, 50844-932-22, 50844-932-51
- Packager: L.N.K. International, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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 you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
SOUNDBODY™
*Compare to the active
ingredient in Benadryl®
Allergy ULTRATAB® TabletsNDC 50844-932-12
Allergy Relief
Diphenhydramine HCl 25 mg, AntihistamineRELIEVES: Sneezing, Runny Nose,
Itchy Throat & Itchy, Watery Eyes100 TABLETS
Actual Size
TAMPER 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 Benadryl® Allergy ULTRATAB®
Tablets. 50844 REV0721D32912Manufactured for Big Lots Stores, Inc.
by LNK INTERNATIONAL, INC.
60 Arkay Drive, Hauppauge, NY 11788 USA
V#733000 ITEM#022732912Sound Body 44-329
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50844-932 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color pink Score no score Shape OVAL Size 11mm Flavor Imprint Code 44;329 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50844-932-22 4 in 1 CARTON 03/02/1990 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:50844-932-12 1 in 1 CARTON 03/02/1990 2 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:50844-932-51 365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/02/1990 4 NDC:50844-932-08 2 in 1 CARTON 03/02/1990 09/21/2019 4 12 in 1 BLISTER PACK; 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 03/02/1990 Labeler - L.N.K. International, Inc. (038154464) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(50844-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(50844-932) , pack(50844-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(50844-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(50844-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(50844-932)