MINI PEACH LIP BALM- shea butter cream

MINI PEACH LIP BALM by

Drug Labeling and Warnings

MINI PEACH LIP BALM by is a Otc medication manufactured, distributed, or labeled by TONYMOLY CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Shea Butter 15.0%

INACTIVE INGREDIENT

Inactive Ingredient: Petrolatum, Diisostearyl Malate, Carthamus Tinctorius (Safflower) Seed Oil, Dipentaerythrityl Hexahydroxystearate/Hexastearate/Hexarosinate, Beeswax, Ceresin, Fragrance, Sorbitan Sesquioleate, Copernicia Cerifera (Carnauba) Wax, Paraffin, Tocopheryl Acetate, Polyglyceryl-2 Triisostearate, Water, Sodium Hyaluronate, Ceramide 3, Rosa Canina Fruit Oil, Butylene Glycol, Lanolin wax, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Alcohol, Prunus Persica (Peach) Fruit Extract, Hamamelis Virginiana (Witch Hazel) Extract, CI 19140:1, CI 15850, Butylparaben, Phenoxyethanol

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings: For external use only When using this product do not get into eyes Stop use and ask a doctor if rash occurs Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Use

Use: Helps prevent and relieve chapped or cracked skin

Directions

Directions: - Clean the skin thoroughly before using - Apply in daily skin care routine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MINI PEACH LIP BALM 
shea butter cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59078-315
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Shea Butter (UNII: K49155WL9Y) (Shea Butter - UNII:K49155WL9Y)	Shea Butter	1.05 g  in 7 g

Inactive Ingredients
Ingredient Name	Strength
Petrolatum (UNII: 4T6H12BN9U)
Diisostearyl Malate (UNII: QBS8A3XZGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59078-315-02	1 in 1 CARTON	05/01/2016
1	NDC: 59078-315-01	7 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2016

Labeler - TONYMOLY CO.,LTD (688216798)

Registrant - TONYMOLY CO.,LTD (688216798)

Establishment
Name	Address	ID/FEI	Business Operations
TONYMOLY CO.,LTD		688216798	manufacture(59078-315)