Label: CVS MAXIMUM STRENGTH ITCH RELIEF- diphenhydramine hydrochloride gel
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-048-69 - Packager: CVS Pharmacy
- 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 April 27, 2012
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only
Do not use - on large areas of the body
- with any other product containing diphenhydramine,
even one taken by mouth
Ask a doctor before use - on chicken pox - on measles
When using this product avoid contact with the eyes
Stop use and ask a doctor if condition worsens,
or if the symptoms persist for more than 7 days
or clear up and occur again within a few days.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CVS MAXIMUM STRENGTH ITCH RELIEF
diphenhydramine hydrochloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 20.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) SODIUM CITRATE (UNII: 1Q73Q2JULR) HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-048-69 118 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part336 08/10/2011 Labeler - CVS Pharmacy (062312574) Registrant - Pharma Pac, LLC (140807475) Establishment Name Address ID/FEI Business Operations Pharma Pac, LLC 140807475 manufacture