OTC Medication Information: M-Rose Seaweed Hydrogel Mask

M-ROSE SEAWEED HYDROGEL MASK — allantoin patch
Beauty Line 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.

allantoin

water, butylene glycol, sea water, xanthan gum, hydrolyzed collagen, calcium lactate, polyglutamic acid, etc

skin protectant

keep out or reach of the children

1. First, cleanse your face and apply serum and emulsion. Then place the mask pack over the entire forehead nose to a thickness of about 1 mm.
2. Smooth along the jaw line.
3. Place over the cheeks and around the mouth. When the mask has completely dried (approximately 15-20 minutes), gently peel off from the chin.
4. Press the face with both palms from the center toward the outer edge of the face, pressing the skin lightly.
5. With fingertips, press on the areas around the eyes and the mouth, starting from the center of the face and moving outward.

-If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
-This product is for exeternal use only. Do not use for internal use
-If possible, avoid direct sunlight and store in cool and area of low humidity
-In order to maintain the quality of the product and avoid misuse
-Avoid placing the product near fire and store out in reach of children

for external use only

package label
(click image for full-size original)
M-ROSE SEAWEED HYDROGEL MASK
allantoin patch
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69327-9001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (ALLANTOIN) ALLANTOIN 0.2 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
BUTYLENE GLYCOL
HYALURONATE SODIUM
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69327-9001-2 4 PACKAGE (PACKAGE) in 1 BOX contains a PACKAGE (69327-9001-1)
1 NDC:69327-9001-1 25 g in 1 PACKAGE This package is contained within the BOX (69327-9001-2)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 10/25/2014
Labeler — Beauty Line Co., Ltd. (688528938)
Registrant — Beauty Line Co., Ltd. (688528938)
Establishment
Name Address ID/FEI Operations
Jincostech Co.,Ltd. 688484870 manufacture (69327-9001)

Revised: 10/2014 Beauty Line Co., Ltd.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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