SNAP CLEAN HANDS LAKESIDE- alcohol aerosol, spray

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Available from:

Cosmetic Specialty Labs, Inc.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antimicrobial Hand Sanitizer to help reduce bacteria on the skin. Stop use and ask a doctor if irritation or rash appears and lasts.

Authorization status:

OTC monograph not final

Summary of Product characteristics

SNAP CLEAN HANDS LAKESIDE- ALCOHOL AEROSOL, SPRAY
COSMETIC SPECIALTY LABS, 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._
----------
ACTIVE INGREDIENT
SD Alcohol 40 75%
Antimicrobial
USE
Hand Sanitizer to help reduce bacteria on the skin.
WARNINGS
FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. FOR EXTERNAL USE ONLY.
WHEN USING THIS PRODUCT do not use in or near the eyes. In case of
contact, rinse
eyes thoroughtly with water.
STOP USE AND ASK A DOCTOR IF irritation or rash appears and lasts.
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or
contact a Poison
Center right away.
DIRECTIONS
Use enough product in your palm to cover hands and rub hands together
biskly until
dry.
Children under 6 years of age should be supervised when using this
product.
OTHER INFORMATION
Store below 110F (43C)
May discolor fabrics or surfaces
INACTIVE INGREDIENTS
Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Fragrance, Glycerin,
Phenoxyethanol,
Polysorbate-20, Purified Water, Tocopheryl Acetate.
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
SNAP CLEAN HANDS LAKESIDE
alcohol aerosol, spray
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:58133-964
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
75 mL in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:58133-
964-02
1 in 1 BOX
09/23/2022
1
40 mL in 1 BOTTLE, SPRAY; Type 0: Not a
Combination Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR