Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
- NDC Code(s): 37808-932-08, 37808-932-78
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 26, 2024
If you are a consumer or patient please visit this version.
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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?
-
Principal display panel
Compare to Benadryl®Allergy ULTRATAB®
Tablets active ingredient*NDC 37808-932-08
H-E-B®
Allergy Relief
Diphenhydramine HCl, 25 mg
AntihistamineAllergy
Relief of:
• Sneezing
• Runny nose
• Itchy, watery eyes
• Itchy throat24 TABLETS
actual size
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT
IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING100% If you aren't completely pleased
GUARANTEE | with this product, we'll be happy to
promise replace it or refund your money.
You have our word on it.*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the
registered trademark Benadryl® Allergy ULTRATAB®
Tablets.50844 REV0721B32908
MADE WITH PRIDE AND CARE FOR H-E-B®, SAN ANTONIO, TX 78204
HEB 44-329
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-932 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:37808-932-08 2 in 1 CARTON 03/02/1990 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37808-932-78 600 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/02/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 03/02/1990 Labeler - H E B (007924756) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(37808-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(37808-932) , pack(37808-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(37808-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(37808-932) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(37808-932)