Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
- NDC Code(s): 21130-329-06, 21130-329-08, 21130-329-12, 21130-329-22
- Packager: Better Living Brands, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated August 2, 2023
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- 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?
-
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care®Quality Guaranteed
VALUE PACK
Compare to Benadryl®
Allergy ULTRATAB® Tablets
active ingredient**NDC 21130-329-06
Allergy Relief
Diphenhydramine HCl 25 mg
Antihistamine• Relief of:
Sneezing, runny nose, itchy
throat & itchy, watery eyesActual Size
200 MINITABS
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, distributors of
Benadryl® Allergy ULTRATAB® Tablets.
50844 REV0721E32906DISTRIBUTED BY
BETTER LIVING BRANDS LLC
P.O. BOX 99, PLEASANTON, CA 94566-0009
1-888-723-3929
www.betterlivingbrandsLLC.comOUR PROMISE
QUALITY & SATISFACTION
100% GUARANTEED
OR YOUR MONEY BACK.Signature Care 44-329
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-329 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:21130-329-08 2 in 1 CARTON 03/02/1990 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:21130-329-22 4 in 1 CARTON 03/02/1990 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:21130-329-12 1 in 1 CARTON 03/02/1990 3 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:21130-329-06 1 in 1 CARTON 03/02/1990 4 200 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 03/02/1990 Labeler - Better Living Brands, LLC (009137209) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(21130-329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(21130-329) , pack(21130-329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(21130-329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(21130-329) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(21130-329)