SHEDIARY TURMERIC FACE CREAM lotion

shediary turmeric face cream by

Drug Labeling and Warnings

shediary turmeric face cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Zhumeng Times Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Sorbitol 5%

Purpose

TIGHTENING AND REJUVENATINGACNE MOISTURIZING

Uses

After cleansing andtoning, take an appropriate amount ofthis product and apply it evenly on theface, massage until absorbed

Warnings

This product is for external useonly, if it gets into your eyes, pleasewash it off with clean water immedi-ately and keep it out of the reach ofchildren.

Dosage and administration

For external use only.

Do not use

Stop use and ask a doctor if

chest pain, rapid heartbeat, faintness, or dizziness occurs

sudden, unexplained weight gain occurs

your hands or feet swell

scalp irritation or redness occurs

unwanted facial hair growth occurs

you do not see hair regrowth in 4 months

May be harmful if used when pregnant or breast-feeding.

Keep out of reach of children, lf swallowed, get medical help or contact a Poison Control Center right away.

When using section

After cleansing andtoning, take an appropriate amount ofthis product and apply it evenly on theface, massage until absorbed

stop use

Broken or inflamed body

Keep out of reach of children

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

Inactive ingredients

Water, MineralOil, Dimethicone, Cetearyl Alcohol,Glyceryl Stearate, Glycerin, Peg-100Stearate,Lauric/myristic/pal-mitic/stearic Glycerides, Phenoxyetha-nol, Cocos Nucifera(coconut) FruitOil, Trehalose,Carbomer, Maltitol.Mannitol, Methylparaben, sodiumPolyacrylate, Ethylhexylglycerin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SHEDIARY TURMERIC FACE CREAM 
shediary turmeric face cream lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84372-048
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SORBITOL (UNII: 506T60A25R) (SORBITOL - UNII:506T60A25R)	SORBITOL	5 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE 6 (UNII: RB8V8W9FQN)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MANNITOL (UNII: 3OWL53L36A)
SODIUM (UNII: 9NEZ333N27)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PEG-100 STEARATE (UNII: YD01N1999R)
MALTITOL (UNII: D65DG142WK)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MINERAL OIL (UNII: T5L8T28FGP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
COCONUT OIL (UNII: Q9L0O73W7L)
WATER (UNII: 059QF0KO0R)
TREHALOSE (UNII: B8WCK70T7I)
METHYLPARABEN (UNII: A2I8C7HI9T)
LAURIC/MYRISTIC DIETHANOLOLAMIDE (UNII: KB1BQB7R06)
IVERMECTIN (UNII: 8883YP2R6D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84372-048-01	30 mL in 1 BOX; Type 0: Not a Combination Product	09/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/09/2024

Labeler - Shenzhen Zhumeng Times Technology Co., Ltd. (631852731)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Zhumeng Times Technology Co., Ltd.		631852731	manufacture(84372-048)