Label: GOOD SENSE ALLERGY RELIEF- diphenhydramine hydrochloride tablet
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NDC Code(s):
0113-0479-53,
0113-0479-62,
0113-0479-67,
0113-0479-78, view more0113-0479-79
- Packager: L. Perrigo Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 26, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Do not use
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- to make a child sleepy
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- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if you have
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- a breathing problem such as emphysema or chronic bronchitis
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- glaucoma
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- trouble urinating due to an enlarged prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
GOOD SENSE ALLERGY RELIEF
diphenhydramine hydrochloride tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0479 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 CARNAUBA WAX (UNII: R12CBM0EIZ) CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK) D&C RED NO. 27 (UNII: 2LRS185U6K) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYSORBATE 80 (UNII: 6OZP39ZG8H) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) Product Characteristics Color PINK (dark) Score no score Shape OVAL Size 10mm Flavor Imprint Code L479;25 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-0479-78 1 in 1 CARTON 10/06/1993 1 100 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0113-0479-62 1 in 1 CARTON 08/20/1991 2 24 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0113-0479-79 400 in 1 BOTTLE; Type 0: Not a Combination Product 02/26/2001 4 NDC:0113-0479-53 12 in 1 CARTON 08/10/2016 03/31/2021 4 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:0113-0479-67 48 in 1 CARTON 06/04/2021 06/04/2021 5 1 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 final part341 08/20/1991 Labeler - L. Perrigo Company (006013346)