OTC Medication Information: Dr.Bellca Hand Sanitizer Gel

DR.BELLCA HAND SANITIZER GEL- alcohol gel
Oneskin Cosmetics Co., Ltd.

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.

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 thoroughly 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 Poision Control Center right away.

Ethyl Alcohol 70%

Antimicrobial

  • Hand sanitizer to help reduce bacteria on the skin.

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Childern under 6 years of age should be supervised when using Dr.Bellca Hand Sanitizer.

Store below 110oF (43oC).
May discolor certain fabrics or surfaces.


Water, Glycerin, Carbomer, Tetrahydroxypropyl Ethylenediamine, Orange Oil, Peppermint Oil, Sodium Hyaluronate, Allantoin, Mugwort Extract, Green Tea Extract.

Dr.Bellca Hand Sanitizer Gel 500mL

DR.BELLCA HAND SANITIZER GEL
hand sanitizer gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70889-800
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.7 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
CARBOMER 940
EDETOL
ORANGE OIL
PEPPERMINT OIL (PEPPERMINT)
HYALURONATE SODIUM
ALLANTOIN
ARTEMISIA PRINCEPS LEAF
GREEN TEA LEAF
WATER
Product Characteristics
Color Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70889-800-01 500 mL in 1 BOTTLE, PUMP None
2 NDC:70889-800-02 236 mL in 1 BOTTLE, PUMP None
3 NDC:70889-800-03 1 TUBE in 1 BOX contains a TUBE
3 50 mL in 1 TUBE This package is contained within the BOX (70889-800-03)
Image of Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/23/2020
Labeler — Oneskin Cosmetics Co., Ltd. (689846630)
Registrant — Oneskin Cosmetics Co., Ltd. (689846630)
Establishment
Name Address ID/FEI Operations
Oneskin Cosmetics Co., Ltd. 689846630 manufacture (70889-800)

Revised: 04/2020 Oneskin Cosmetics Co., Ltd.

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.

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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