SULFUR ANTI-MITE SHOWER GEL (sodium laureth sulfat,decyl glucoside,palm kernelamide dea,cocamidopropyl betaine,lonicera japonica- honeysuckle flower extract,colloidal sulfur. liquid

Sulfur anti-mite shower gel by

Drug Labeling and Warnings

Sulfur anti-mite shower gel by is a Otc medication manufactured, distributed, or labeled by Guangdong Junhui Biotechnology Co., Ltd, Dongguan Xiaogoubeige trading company Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Sodium Laureth Sulfate 8.4%
Decyl Glucoside 1.7%
Palm Kernelamide DEA 1%
Cocamidopropyl Betaine 1%
Lonicera Japonica(Honeysuckle) Flower Extract 3.5%
Colloidal Sulfur 0.2%

Purpose

Moisturise
Cleansing
Antibacterial

Uses

Apply an appropriate amount to the palm of your hand or bathing utensil with water to form a lather and gently lather over the body, then rinse off with water.

Warnings

For external use only.Avoid contact with eyes.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

CAUTION

After using the product if irritation or rash appears,discontinue use.If irritation or
rash persists.consult your doctor.

Product Name

Sulfur anti-mite shower gel

DOSAGE

Approximately 0.2-0.4 oz each time.

Inactive Ingredients

Water,Sodium Chloride,Glycerin,Glycol Distearate, Fragrance, DMDM Hydantoin, Citric Acid,Butylene Glycol,Magnesium Nitrate, Hydroxyacetophenone.Methylchloroisothiazolinone, Kl5, Kl4, Magnesium Chloride,Glycine, Methylisothiazolinone,Serine, Glutamic Acid, Aspartic Acid, Leucine,Alanine,Lysine,Arginine,Tyrosine,Phenylalanine.Threonine, Proline, Valine,lsoleucine, Histidine

Manufacturer

Guangdong Junhui Biotechnology Co.,LTD

Address

No.10,Guangrui Street,Guangzhou(Qingyuan) Industrial Transfer Park,Shijiao Town,Qingcheng District,
Qingyuan City,Guangdong Province,China

Capacity

300ml-e-10.1f1.oz

Shelf Life

3 Years

Place of Origin

Made in China

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SULFUR ANTI-MITE SHOWER GEL 
sodium laureth sulfat,decyl glucoside,palm kernelamide dea,cocamidopropyl betaine,lonicera japonica(honeysuckle) flower extract,colloidal sulfur. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84509-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM (UNII: 9NEZ333N27) (SODIUM - UNII:9NEZ333N27)	SODIUM	25200 mg  in 300 mL
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) (LONICERA JAPONICA FLOWER - UNII:4465L2WS4Y)	LONICERA JAPONICA FLOWER	10500 mg  in 300 mL
DECYL GLUCOSIDE (UNII: Z17H97EA6Y) (DECYL GLUCOSIDE - UNII:Z17H97EA6Y)	DECYL GLUCOSIDE	5100 mg  in 300 mL
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) (COCAMIDOPROPYL BETAINE - UNII:5OCF3O11KX)	COCAMIDOPROPYL BETAINE	3000 mg  in 300 mL
PALM KERNEL OIL (UNII: B0S90M0233) (PALM KERNEL OIL - UNII:B0S90M0233)	PALM KERNEL OIL	3000 mg  in 300 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	600 mg  in 300 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
LEUCINE (UNII: GMW67QNF9C)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
ISOLEUCINE (UNII: 04Y7590D77)
PROLINE (UNII: 9DLQ4CIU6V)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
HISTIDINE (UNII: 4QD397987E)
SERINE (UNII: 452VLY9402)
GLYCINE (UNII: TE7660XO1C)
GLUTAMIC ACID (UNII: 3KX376GY7L)
LYSINE (UNII: K3Z4F929H6)
PHENYLALANINE (UNII: 47E5O17Y3R)
FRAGRANCE 13576 (UNII: 5EM498GW35)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
KI5 (UNII: H77VEI93A8)
WATER (UNII: 059QF0KO0R)
ACONITIC ACID (UNII: 93371T1BXP)
KI4 (UNII: I753WB2F1M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALANINE (UNII: OF5P57N2ZX)
THREONINE (UNII: 2ZD004190S)
GLYCERIN (UNII: PDC6A3C0OX)
VALINE (UNII: HG18B9YRS7)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
ASPARTIC ACID (UNII: 30KYC7MIAI)
TYROSINE (UNII: 42HK56048U)
ARGININE (UNII: 94ZLA3W45F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84509-034-01	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/23/2024

Labeler - Guangdong Junhui Biotechnology Co., Ltd (707735253)

Registrant - Dongguan Xiaogoubeige trading company Ltd. (707735253)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Xiaogoubeige trading company Ltd.		707735253	label(84509-034) , manufacture(84509-034)