IC IVY RELIEF- diphenhydramine hydrochloride and zinc acetate liquid

IC Ivy Relief by

Drug Labeling and Warnings

IC Ivy Relief by is a Otc medication manufactured, distributed, or labeled by R & R Lotion, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

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

Uses

Temporary relieves pain and itching associated with: Insect Bites

• Minor Burns
• Minor Cuts
• Sunburn
• Minor Skin Irritations
• Scrapes
• Dries oozing and weeping of Poison Ivy, Poison Oak, and Poison Sumac
• Rashes due to Poison Ivy, Poison Oak, and Poison Sumac.

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 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

• 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

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) ℮

INGREDIENTS AND APPEARANCE

IC IVY RELIEF 
diphenhydramine hydrochloride and zinc acetate liquid

Product 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)