GZE HONEY MILK HAND WAX- beeswax 5% honey extract 5% paste

GZE HONEY MILK HAND WAX by

Drug Labeling and Warnings

GZE HONEY MILK HAND WAX by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yilong Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

Water

Polyvinyl Alcohol

Parfum

Sodium Polyacrylate

Ethylhexyl Stearate

Diazolidinyl Urea

Trideceth-6

1,2-Butanediol

Glycerin

CI 19140

ACTIVE INGREDIENT

Beewax

Honey Extract

PURPOSE

Exfoliation.

INDICATIONS & USAGE

Apply hand wax and spread a uniform layer of about 1 mm thick with a spoon.Wait 15-20 minutes, then remove the hardened film from your hands.

WARNINGS

For external use only.

STOP USE

Stop use and ask a doctor if rash occurs.

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

When using this product keep out of eyes. Rinse with water to remove.

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

Apply hand wax and spread a uniform layer of about 1 mm thick with a spoon.Wait 15-20 minutes, then remove the hardened film from your hands.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GZE HONEY MILK HAND WAX 
beeswax 5% honey extract 5% paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74458-058
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HONEY EXTRACT (UNII: Y9H1V576FH) (HONEY EXTRACT - UNII:Y9H1V576FH)	HONEY EXTRACT	5 g  in 100 g
BEESWAX (UNII: 2ZA36H0S2V) (BEESWAX - UNII:2ZA36H0S2V)	BEESWAX	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,2-BUTANEDIOL (UNII: RUN0H01QEU)
POLYVINYL ALCOHOL (UNII: 532B59J990)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
GLYCERIN (UNII: PDC6A3C0OX)
CI 19140 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74458-058-01	120 g in 1 JAR; Type 0: Not a Combination Product	06/10/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M030	06/10/2024

Labeler - Guangzhou Yilong Cosmetics Co., Ltd (420929116)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yilong Cosmetics Co., Ltd		420929116	manufacture(74458-058)