Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
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NDC Code(s):
11822-0329-1,
11822-0329-2,
11822-0329-3,
11822-0329-4, view more11822-0329-5, 11822-0329-6, 11822-0329-7, 11822-0329-8, 11822-0329-9
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 6, 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
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- difficulty in urination due to enlargement of the prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to the active ingredient in
Benadryl® Allergy ULTRATAB® Tablets*NDC 11822-0329-8
ALLERGY RELIEF
DIPHENHYDRAMINE HCl 25 mgANTIHISTAMINE
RELIEF OF
Sneezing • Runny nose
Itchy, watery eyes
Itchy throatACTUAL SIZE
24
MINITABS
25 mg EACH
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS
OPENED OR IF BLISTER UNIT IS TORN, BROKEN
OR SHOWS ANY SIGNS OF TAMPERING
*This product is not
manufactured or distributed
by Johnson & Johnson
Corporation, owner of the
registered trademark
Benadryl® Allergy
ULTRATAB® Tablets.
50844 REV0721H32908DISTRIBUTED 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 44-329
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0329 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:11822-0329-8 2 in 1 CARTON 03/02/1990 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11822-0329-4 4 in 1 CARTON 03/02/1990 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:11822-0329-2 1 in 1 CARTON 03/02/1990 3 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:11822-0329-6 1 in 1 CARTON 03/02/1990 4 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:11822-0329-1 365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/02/1990 6 NDC:11822-0329-5 1 in 1 CARTON 03/02/1990 10/08/2021 6 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:11822-0329-7 3 in 1 CARTON 03/02/1990 09/09/2017 7 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 8 NDC:11822-0329-3 1 in 1 PACKAGE 03/02/1990 10/08/2019 8 10 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 9 NDC:11822-0329-9 1 in 1 CARTON 03/02/1990 10/16/2021 9 2 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 - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(11822-0329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(11822-0329) , pack(11822-0329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(11822-0329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(11822-0329)