I.C. IVY BLOCK- zinc acetate lotion

I.C. Ivy Block by

Drug Labeling and Warnings

I.C. Ivy Block 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 Ingredients

Zinc Acetate 0.1%

Purpose

Skin Protectant

Uses

Poison Ivy, Oak, Sumac Protectant

Warnings

For external use only - When using this product

• do not get into eyes
• If contact occurs, rinse eyes thoroughly with water
• Stop use and ask a doctor if condition worsens
• Symptoms last 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.

Directions

Shake well before use

• Apply 15 minutes before exposure
• Apply generously to dry, exposed skin
• Allow to dry
• Apply every 4 hours for continued protection or sooner if needed
• After possible exposure with skin irritants, remove using IC Ivy Cleanser
• Children under 2 year - ask a doctor.

Other Information

Protect from excessive heat (48°C/120°F)

Inactive Ingredients

Di Water, Cyclopentasiloxane (and) Quaternium - 90 Bentonite (and) Trifluoromethyl C1-4 Alkyl Dimethicone (and) Propylene Carbonate, Bentonite, Dimethicone, Polyacrylamide (and) c13-14 Isoparaffin (and) Laureth-7, Glycerin, Magnesium Aluminum Silicate, Phenoxyethanol (and) Ethylhexlglycerin, PVP, Aloe Barbadensis Leaf Juice, Disodium EDTA, Hamamelis Virginiana (Witch Hazel) Water (and) Phenoxyethanol, Citric Acid

Questions or Comments?

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PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label

I.C.®
Ivy Block

R&R LOTION
USA

Pre Contact
Formula

4oz. (118ml) ℮

INGREDIENTS AND APPEARANCE

I.C. IVY BLOCK 
zinc acetate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
QUATERNIUM-90 (UNII: BE5VYX4VP8)
BENTONITE (UNII: A3N5ZCN45C)
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)
GLYCERIN (UNII: PDC6A3C0OX)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-200-03	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/21/2021
2	NDC: 59555-200-04	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/21/2021
3	NDC: 59555-200-07	118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/21/2021
4	NDC: 59555-200-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/21/2021
5	NDC: 59555-200-10	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/21/2021
6	NDC: 59555-200-11	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/21/2021
7	NDC: 59555-200-01	5 mL in 1 PACKET; Type 0: Not a Combination Product	09/21/2021
8	NDC: 59555-200-16	4 mL in 1 PACKET; Type 0: Not a Combination Product	09/21/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/21/2021

Labeler - R & R Lotion, Inc (062979000)