Richway Amethyst Hydrogel Face Mask by R&L Co., Ltd. / R&L Co., Ltd. Drug Facts

Richway Amethyst Hydrogel Face Mask by

Drug Labeling and Warnings

Richway Amethyst Hydrogel Face Mask by is a Otc medication manufactured, distributed, or labeled by R&L Co., Ltd., R&L Co., Ltd. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RICHWAY AMETHYST HYDROGEL FACE MASK- glycerin liquid 
R&L Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

glycerin

water, butylene glycol, etc.

skin protectant

keep out of reach of the children

apply maks to lean face
leave the mask on your face about 20 minutes until it begins to dry

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

for external use only

RICHWAY AMETHYST HYDROGEL FACE MASK 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70099-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70099-0002-1	22 g in 1 PACKAGE; Type 0: Not a Combination Product	10/10/2017	10/30/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	08/31/2015	10/30/2019

Labeler - R&L Co., Ltd. (689036771)

Registrant - R&L Co., Ltd. (689036771)

Establishment
Name	Address	ID/FEI	Business Operations
R&L Co., Ltd.		689036771	manufacture(70099-0002)

Revised: 10/2019

Document Id: 9618b94f-78f9-f0de-e053-2a95a90a7dde

34390-5

Set id: ddf0da35-35af-4650-a861-cfe26ec7ac56

Version: 2

Effective Time: 20191029