HANNA HAND SANITIZER GEL- alcohol gel

HANNA HAND SANITIZER gel by

Drug Labeling and Warnings

HANNA HAND SANITIZER gel by is a Otc medication manufactured, distributed, or labeled by Rainbow Beauty Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol

INACTIVE INGREDIENT

Water, Glycerin, Carbomer, Triethanolamine, Fragrance, Camellia Sinensis Leaf Extract, Butylene Glycol, Aloe Barbadensis Leaf Extract, Portulaca Oleracea Extract, Centella Asiatica Extract, Pinus Densiflora Extract, CI 19140, CI 42090

PURPOSE

Sterilization of hands and skin

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Apply an appropriate amount on your hands and rub well to dry.

WARNINGS

1. Do not use on the following body parts. A wide range of body parts and damaged skin around the eyes and
ears, in the oral cavity (may have irritating effects)
2. If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.
1) Hypersensitivity symptoms such as rash, erythema, itching, and edema
2) Skin irritation symptoms
3. Other precautions
1) For external use only (do not underwear).
2) Be careful not to get into your eyes, and if so, rinse well with clean water and consult a doctor or pharmacist.
3) Be careful not to inhale the vapor when using it extensively or for a long period of time (irritation to the
mucous membranes, headaches, etc. may occur if ethanol vapor is consumed in large quantities or repeatedly).
4) If repeated use on the same site, be careful as the skin may become rough due to degreasing.
5) Do not use sealed bandages, cast bandages, packs, etc., as irritation may occur.
6) Do not use this medicine for anal or vaginal compresses as it may cause irritation or chemical burns.
7) Do not use for any other purpose.
4. Precautions for storage
1) Avoid shading and keep in shading.
2) Keep it out of reach of children, and if a child swallows it, go to the hospital right away.
3) After use, close the product completely with a lid to prevent the product from drying out or entering foreign
Objects.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANNA HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71193-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PURSLANE (UNII: M6S840WXG5)
TROLAMINE (UNII: 9O3K93S3TK)
PINUS DENSIFLORA BARK (UNII: U68X322T49)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
D&C BLUE NO. 4 (UNII: 0KSY80VYS3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71193-101-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/03/2020
2	NDC: 71193-101-02	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/03/2020

Labeler - Rainbow Beauty Cosmetic Co., Ltd. (695684820)

Registrant - Rainbow Beauty Cosmetic Co., Ltd. (695684820)

Establishment
Name	Address	ID/FEI	Business Operations
Rainbow Beauty Cosmetic Co., Ltd.		695684820	manufacture(71193-101) , label(71193-101)