Label: DIPHENHYDRAMINE HYDROCHLORIDE capsule
- NDC Code(s): 60760-697-30
- Packager: ST. MARY'S MEDICAL PARK PHARMACY
- This is a repackaged label.
- Source NDC Code(s): 0904-7237
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 18, 2023
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- Drug Facts
- PURPOSE
- Uses
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WARNINGS
Ask a doctor before use if you have
a breathing problem such as emphysema or chronic bronchitis glaucoma
trouble urinating due to an enlarged prostate gland - Directions
- Other information
- INACTIVE INGREDIENT
- Questions or comments?
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SPL UNCLASSIFIED SECTION
Distributed by: MAJOR® PHARMACEUTICALS, Indianapolis, IN 46268
Product of China. Manufactured and packaged in the USA using domestic and imported ingredients.
*This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Benadryl®.
To preserve quality and freshness, keep bottle tightly closed.
KEEP OUT OF REACH OF CHILDREN. DO NOT USE IF PRODUCT APPEARS TO BE
TAMPERED WITH OR IMPRINTED SEAL UNDER CAP IS BROKEN OR MISSING.
DO NOT USE IF RED CAPSULE BAND IS BROKEN OR MISSING. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIPHENHYDRAMINE HYDROCHLORIDE
diphenhydramine hydrochloride capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60760-697(NDC:0904-7237) 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 D&C RED NO. 28 (UNII: 767IP0Y5NH) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) GELATIN (UNII: 2G86QN327L) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) SODIUM LAURYL SULFATE (UNII: 368GB5141J) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color pink (Half pink and half clear with white powder inside and sealed with red band) Score no score Shape CAPSULE Size 14mm Flavor Imprint Code CPC;835 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60760-697-30 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/14/2022 Labeler - ST. MARY'S MEDICAL PARK PHARMACY (063050751) Establishment Name Address ID/FEI Business Operations ST. MARY'S MEDICAL PARK PHARMACY 063050751 relabel(60760-697) , repack(60760-697)