LOLLIPOP SCENTED ANTI-BACTERIAL HAND GEL- ethyl alcohol gel

lollipop scented by

Drug Labeling and Warnings

lollipop scented by is a Otc medication manufactured, distributed, or labeled by Nantong Health & Beyond Hygienic Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol, 65% v/v

PURPOSE

Purpose  Antimicrobial

INDICATIONS & USAGE

Uses  hand sanitizer to help

reduce bacteria on skin

WARNINGS

Warnings

For external use only.

Flammable, keep away

from fire or flame.

Do not use in or near the eyes

In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation, excessive redness

or rash develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of

children. If swallowed, get

medical help or contact a Poison

Control Center right away.

DOSAGE & ADMINISTRATION

Directions  Put a dime sized

drop onto hands and rub

together briskly ntil dry.

STORAGE AND HANDLING

Other information

Store below 110° F (43° C)

INACTIVE INGREDIENT

Inactive ingredients

water, glycerin, propylene

glycol, fragrance, carbomer,

triethanolamine, blue 1, red

33, yellow 5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LOLLIPOP SCENTED  ANTI-BACTERIAL HAND GEL
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43473-814
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color		Score
Shape		Size
Flavor	FRUIT (Lollipop)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43473-814-01	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/12/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/12/2017

Labeler - Nantong Health & Beyond Hygienic Products Inc. (421280161)