OTC Medication Information: HUANGJISOO HAND SANITIZER

HUANGJISOO HAND SANITIZER- alcohol gel
Newfeel

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

Active ingredients: Ethyl Alcohol 70%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin, Carbomer, 1,2-Hexanediol, Apium Graveolens (Celery) Extract, Daucus Carota Sativa (Carrot) Root Extract, Foeniculum Vulgare (Fennel) Seed Extract, Brassica Oleracea Acephala Leaf Extract, Coriandrum Sativum (Coriander) Extract, Lactuca Scariola Sativa (Lettuce) Leaf Extract, Spinacia Oleracea (Spinach) Leaf Extract

PURPOSE

Purpose: Antiseptic

WARNINGS

Warnings:
For external use only : hands
Flammable, keep away from fire or flame.
When using this product ■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin. ■ do not inhale or ingest
Stop use and ask a doctor if ■irritation and redness develop ■ condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

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.

Uses

Uses:
■ for handwashing to decrease the bacteria on the skin
■ recommended for repeated use

Directions

Directions:

■ wet hands thoroughly with product and allow to dry without wiping

■ for children under 6, use only under adult supervision

■ not recommended for infants

Other information

Other information


■ do not store above 105℉

■ may discolor some fabrics

■ harmful to wood finishes and plastics

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

HUANGJISOO HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73713-030
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 350 mL in 500 mL
Inactive Ingredients
Ingredient Name Strength
Water
Glycerin
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
1,2-Hexanediol
CELERY
CARROT
FENNEL SEED
KALE
CORIANDER
LETTUCE
SPINACH
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73713-030-01 500 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 04/01/2020
Labeler — Newfeel (690062383)
Registrant — Newfeel (690062383)
Establishment
Name Address ID/FEI Operations
Newfeel 690062383 manufacture (73713-030)

Revised: 04/2020 Newfeel

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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