Label: ALLERGY RELIEF DIPHENHYDRAMINE HCL- diphenhydramine hydrochloride capsule, liquid filled
- NDC Code(s): 70000-0585-1
- Packager: Cardinal Health 110, LLC. DBA Leader
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each softgel)
- Purpose
- Uses
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Warnings
Do not use •to make a child sleepy
•with any other product containing diphenhydramine, even one used on skinAsk a doctor before use if you have
•a breathing problem such as emphysema or chronic bronchitis •glaucoma
•difficulty in urination due to enlargement to the prostate glandAsk a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
When using this product
•marked drowsiness may occur
•avoid alcoholic beverages
•alcohol, sedatives, and tranquilizers may increase drowsiness
•use caution when driving a motor vehicle or operating machinery
•excitability may occur, especially in childrenIf pregnant or breast-feeding, ask a health professional before use
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
LEADER ™
DYE-FREE
Relief of: Sneezing, Runny Nose, Itchy, Watery Eyes, Itchy Throat
COMPARE TO BENADRYL® DYE-FREE ALLERGY active ingredient*
100% Money Back Guarantee
READ AND KEEP OUTER PACKAGE FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
*This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Benadryl® Dye-Free Allergy.
All LEADERTM Brand Products Have A 100% Money Back Guarantee
Return to place of purchase if not satisfied.DISTRIBUTED BY CARDINAL HEALTH
DUBLIN, OHIO 43017
www.myleader.com 1-800-200-6313
Product of UAE
Packaged and Quality Assured in the USA©2021 Cardinal Health. All Rights Reserved. CARDINAL HEALTH, the Cardinal Health LOGO, LEADER, and the Leader LOGO are trademarks or registered trademarks of Cardinal Health. All other marks are the property of their respective owners.
TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS SIGNS OF TAMPERING
- Packaging
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF DIPHENHYDRAMINE HCL
diphenhydramine hydrochloride capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0585 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 GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SORBITAN (UNII: 6O92ICV9RU) Product Characteristics Color yellow (pale yellow transparent) Score no score Shape OVAL (oblong) Size 15mm Flavor Imprint Code 780 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0585-1 2 in 1 CARTON 09/15/2021 1 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 09/15/2021 Labeler - Cardinal Health 110, LLC. DBA Leader (063997360)