IC IVY RELIEF- diphenhydramine hydrochloride and zinc acetate liquid 
R & R Lotion, Inc

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.

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IC® Ivy Relief

Drug Facts

Active IngredientsPurpose
Diphenhydramine HCL 2%Topical Analgesic
Zinc Acetate 0.1%Skin Protectant

Uses

Temporary relieves pain and itching associated with: Insect Bites

Warnings

For external use only. Do not use on large areas of the body

Ask doctor before use on chicken pox

  • on measles

When using this product avoid contact with eyes

Stop use and ask doctor if conditions worsen, or do not improve within 7 days

  • 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 Poison Control Center right away.

Directions

Do not use more than directed

Other Information

Protect from excessive heat (40ºC/104ºF)

Inactive Ingredients

Propylene Glycol, Xanthan Gum, DI Water, PVP K-30

Questions or Comments?

1-888-860-7424

PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label

I.C.®
Ivy
Relief

R&R LOTION
USA

Kills Germs

2oz. (59ml) ℮

PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label
IC IVY RELIEF 
diphenhydramine hydrochloride and zinc acetate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59555-230
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Zinc Acetate (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) Zinc Acetate1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Xanthan Gum (UNII: TTV12P4NEE)  
Propylene Glycol (UNII: 6DC9Q167V3)  
POVIDONE K30 (UNII: U725QWY32X)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59555-230-181 mL in 1 PACKET; Type 0: Not a Combination Product09/01/2021
2NDC:59555-230-1920 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product09/01/2021
3NDC:59555-230-0459 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
4NDC:59555-230-07118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/01/2021
Labeler - R & R Lotion, Inc (062979000)

Revised: 9/2021
Document Id: 9977d446-e162-4dcb-9926-3be2739d72a1
Set id: 7661cbc8-6b2e-4144-9085-3a58040446f2
Version: 1
Effective Time: 20210924
 
R & R Lotion, Inc