DRUGGIST HONEY HALO- honey halo cream

DRUGGIST HONEY HALO by

Drug Labeling and Warnings

DRUGGIST HONEY HALO by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Tocopherol3% Anti-oxidation
Glycerin7% Moisturizing
Arginine3% Moisturizing
Aloe Perryi Extract5% Moisturizing
Hydrolyzed Rice Extract5% Moisturizing

Purpose

Anti-wrinkle, moisturizes

Uses

Anti-wrinkle, moisturizes, nourishes and repairs skin, keeping skin hydrated, soft and smooth.

Warnings

For external use only
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs
Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

Do not use

Do not use on damaged or broken skin

When using this product

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

Stop use and ask a doctor if

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

Ask Doctor

When Pregnant or breast-feeding.

Directions

1. After cleansing, take appropriate amount of spot lightening cream.
2. Apply evenly to the parts of the face that need moisturizing, and massage gently until completely absorbed.
3. Use once in the morning and once in the evening. Continued use will bring better results.

Other information

Please store in a cool, dry place away from direct sunlight.

Inactive ingredients

Aqua, Decyl Cocoate, Caprylic/Capric Triglyceride, Honey Extract ,
Glyceryl Stearate Citrate , Stearic Acid, Stearyl Alcohol, Zea Mays (corn) Starch,Cetearyl Alcohol, Coco-Glucoside, Magnesium Aluminum Silicate, Xanthan Gum, Sodium Stearoyl Lactylate, Sclerotium Gum, Phenoxyethanol,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DRUGGIST HONEY HALO 
honey halo cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83872-220
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROLYZED ORYZANOL (UNII: 3OE0DD1I5J) (HYDROLYZED ORYZANOL - UNII:3OE0DD1I5J)	HYDROLYZED ORYZANOL	50 mg  in 1 g
ALOE PERRYI LEAF (UNII: DBY89R2TG5) (ALOE PERRYI LEAF - UNII:DBY89R2TG5)	ALOE PERRYI LEAF	50 mg  in 1 g
ARGININE (UNII: 94ZLA3W45F) (ARGININE - UNII:94ZLA3W45F)	ARGININE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83872-220-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/06/2024

Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xiaomai Manufacturing Co., Ltd.		712999147	manufacture(83872-220)