I.C. WATERLESS HAND CLEANER WITH MICRO SCRUBBERS- benzalkonium chloride lotion

I.C. Waterless Hand Cleaner with Micro Scrubbers by

Drug Labeling and Warnings

I.C. Waterless Hand Cleaner with Micro Scrubbers 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

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

Hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only

• When using this product, avoid contact with eyes
• In case of eye contact, flush with water

• Keep out of reach of children, except under adult supervision
• If swallowed, get medical help

• Discontinue use if skin irritation or redness develops

Directions

Rub onto hands and lather vigorously. Dry off hands with towel.

Ingredients

Purified Water, Cetearyl Alcohol (and) Behentrimonium Methosulfate, Glyceryl Stearate (and) PEG-100 Stearate, Caprylic/Capric Triglyceride, Sunflower Butter, Glycerin, Dimethicone, Cetyl Alcohol, Hydrolyzed Jojoba Esters, Gluconolactone (and) Sodium Benzoate, Shea Butter, Synthetic Wax, Xanthan Gum, Disodium EDTA, Propylene Glycol, Vaccinium Macrocarpon (Cranberry) Fruit, Coffea Robusta Seed, Fragaria Vesca (Strawberry) Fruit, Euterpe Oleracea Fruit, Vaccinium Angustifolium (Blueberry) Fruit, Camellia Sinensis (Green Tea) Leaf, Vitis Vinifera (Grape) Seed, Punica (Pomegranate) Granatum Fruit, Rubus Idaeus (Raspberry) Fruit, Potassium Sorbate, Agave Tequilana Leaf (Blue Agave), Simmondsia Chinensis (Jojoba) Seed, Aloe Barbadensis Leaf Juice (Aloe Vera), Vitamin E Acetate, Vitamin A (and) D

PRINCIPAL DISPLAY PANEL - 4 mL Packet Label

I.C. ®
Waterless
Hand
Cleaner
with Micro Scrubbers

4ML
ANTIBACTERIAL

R&R Lotion
Call (480) 443-9255
visit RRlotion.com

LN165_B
NDC# 59555-303-16

INGREDIENTS AND APPEARANCE

I.C. WATERLESS HAND CLEANER WITH MICRO SCRUBBERS 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-303
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
Behentrimonium Methosulfate (UNII: 5SHP745C61)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 MONOSTEARATE (UNII: YD01N1999R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
Glycerin (UNII: PDC6A3C0OX)
Dimethicone (UNII: 92RU3N3Y1O)
Cetyl Alcohol (UNII: 936JST6JCN)
POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)
Gluconolactone (UNII: WQ29KQ9POT)
Sodium Benzoate (UNII: OJ245FE5EU)
Shea Butter (UNII: K49155WL9Y)
Paraffin (UNII: I9O0E3H2ZE)
Xanthan Gum (UNII: TTV12P4NEE)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CRANBERRY (UNII: 0MVO31Q3QS)
ROBUSTA COFFEE BEAN (UNII: V5032728L7)
FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU)
ACAI (UNII: 46AM2VJ0AW)
LOWBUSH BLUEBERRY (UNII: G90PX41VP0)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
VITIS VINIFERA SEED PROANTHOCYANIDINS (UNII: RDS2V6DVY5)
POMEGRANATE (UNII: 56687D1Z4D)
RASPBERRY (UNII: 4N14V5R27W)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)
SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
Cholecalciferol (UNII: 1C6V77QF41)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-303-04	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/09/2025
2	NDC: 59555-303-07	118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/09/2025
3	NDC: 59555-303-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/09/2025
4	NDC: 59555-303-09	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/09/2025
5	NDC: 59555-303-10	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/09/2025
6	NDC: 59555-303-11	3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/09/2025
7	NDC: 59555-303-16	4 mL in 1 PACKET; Type 0: Not a Combination Product	04/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	505G(a)(3)	04/09/2025

Labeler - R & R Lotion, Inc (062979000)

Establishment
Name	Address	ID/FEI	Business Operations
R & R Lotion, Inc		062979000	MANUFACTURE(59555-303)