Label: ALLERGY RELIEF- diphenhydramine hcl capsule, liquid filled
- NDC Code(s): 55910-752-09, 55910-752-12
- Packager: DOLGENCORP INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 25, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each capsule)
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
SPL UNCLASSIFIED SECTION
THIS PRODUCT IS PACKAGED IN A TAMPER EVIDENT PACKAGE.
USE ONLY IF BLISTERS ARE INTACT.KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
†This product is not manufactured or distributed by the owners of Benadryl® Allergy LIQUI-GELS®.
DISTRIBUTED BY OLD EAST MAIN CO.
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072
MADE IN INDIA
Mfg. Lic. No.: TN00002123R0724
L0000890 - 24's count
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-752 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 SORBITAN (UNII: 6O92ICV9RU) GELATIN (UNII: 2G86QN327L) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) Product Characteristics Color white (Clear) Score no score Shape CAPSULE Size 17mm Flavor Imprint Code DF25 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-752-12 2 in 1 CARTON 02/27/2025 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:55910-752-09 4 in 1 CARTON 04/07/2025 2 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 02/27/2025 Labeler - DOLGENCORP INC (068331990) Registrant - Bionpharma Inc. (079637826) Establishment Name Address ID/FEI Business Operations SOFTGEL HEALTHCARE PRIVATE LIMITED 676666501 manufacture(55910-752)

