OTC Medication Information: P1P Magic Whitening Antiaging

P1P MAGIC WHITENING ANTIAGING- niacinamide, panthenol and adenosine liquid
Phytos Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

P1P Magic Whitening & Antiaging

whitening ampoule
(click image for full-size original)

Niacinamide (2.5%) Panthenol (1%) Adenosine (0.04%)

skin protectant

Keep out of reach of children — Do not swallow. In case of accidental ingestion, seek professional assistance.

Moisturizes skin

For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product — Do not apply on other parts of the body — Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. — Do not apply directly to wound or open cut. Stop use and ask doctor if rash or irritation on skin develops and lasts. Store at room temperature

Directions Apply moderate amount gently on face after cleanse

Water, Cetyl Ethylhexanoate,Tranexamic Acid, Centella Asiatica Extract, Bacillus/Soybean Ferment Extract, Salix Alba (Willow) Bark Extract, Morus Alba Bark Extract, Paeonia Suffruticosa Root Extract, Camellia Sinensis Leaf Extract, Oligopeptide-1, Oligopeptide-2, Tremella Fuciformis Sporocarp Extract, Palmitoyl Oligopeptide, Glycosyl Trehalose, Lecithin, Glycerin, 3-O-Ethyl Ascorbic Acid, 1,2-Hexanediol, Panthenol, Tocopheryl Acetate, Polysorbate 80, Poloxamer 407, Dipotassium Glycyrrhizate, Citric Acid, Phytosphingosine Phosphate

P1P MAGIC WHITENING ANTIAGING
niacinamide, panthenol, adenosine liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69579-104
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
niacinamide (NIACINAMIDE) niacinamide 0.025 in 5 mL
PANTHENOL (PANTHENOL) PANTHENOL 0.01 in 5 mL
adenosine (ADENOSINE) adenosine 0.0004 in 5 mL
Inactive Ingredients
Ingredient Name Strength
water
CETYL ETHYLHEXANOATE
TRANEXAMIC ACID
CENTELLA ASIATICA
SALIX ALBA BARK
morus alba bark
PAEONIA SUFFRUTICOSA ROOT
GREEN TEA LEAF
PALMITOYL OLIGOPEPTIDE
EGG PHOSPHOLIPIDS
glycerin
3-O-ETHYL ASCORBIC ACID
1,2-HEXANEDIOL
.ALPHA.-TOCOPHEROL ACETATE
POLYSORBATE 80
POLOXAMER 407
GLYCYRRHIZINATE DIPOTASSIUM
CITRIC ACID MONOHYDRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69579-104-02 5 AMPULE in 1 CARTON contains a AMPULE (69579-104-01)
1 NDC:69579-104-01 5 mL in 1 AMPULE This package is contained within the CARTON (69579-104-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/26/2015
Labeler — Phytos Co., Ltd. (689196775)
Registrant — Phytos Co., Ltd. (689196775)
Establishment
Name Address ID/FEI Operations
Phytos Co., Ltd. 689196775 manufacture (69579-104)

Revised: 02/2015 Phytos 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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