Label: IC IVY RELIEF- diphenhydramine hydrochloride and zinc acetate liquid
- NDC Code(s): 59555-230-04, 59555-230-07, 59555-230-18, 59555-230-19
- Packager: R & R Lotion, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 September 24, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
Do not use more than directed
- Hold stick straight down over infected area
- press tip of stick repeatedly on affect skin area until liquid flows, then dab sparingly
- adults and children 2 years of age and older: apply to affected area not more then 3 to 4 times daily
- children under 2 years of age: ask a doctor
- Other Information
- Inactive Ingredients
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label
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INGREDIENTS AND APPEARANCE
IC IVY RELIEF
diphenhydramine hydrochloride and zinc acetate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59555-230 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 20 mg in 1 mL Zinc Acetate (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) Zinc Acetate 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Xanthan Gum (UNII: TTV12P4NEE) Propylene Glycol (UNII: 6DC9Q167V3) POVIDONE K30 (UNII: U725QWY32X) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59555-230-18 1 mL in 1 PACKET; Type 0: Not a Combination Product 09/01/2021 2 NDC:59555-230-19 20 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 09/01/2021 3 NDC:59555-230-04 59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/01/2021 4 NDC:59555-230-07 118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/01/2021 Labeler - R & R Lotion, Inc (062979000)