MIELLE ILLUMINATING FACE- sunscreen cream

Mielle illuminating face by

Drug Labeling and Warnings

Mielle illuminating face by is a Otc medication manufactured, distributed, or labeled by RNA PHARMA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MIELLE ILLUMINATING FACE 
sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60717-720
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.075 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.05 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.025 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETYL ALCOHOL (UNII: 936JST6JCN)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
STEARETH-20 (UNII: L0Q8IK9E08)
SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
PEA PROTEIN (UNII: 7Q50F46595)
DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
CURDLAN (UNII: 6930DL209R)
ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYETHYLENE GLYCOL 4500 (UNII: TVH7653921)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
DIMETHICONE (UNII: 92RU3N3Y1O)
SHEA BUTTER (UNII: K49155WL9Y)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
POLYISOBUTYLENE (1100000 MW) (UNII: FLT10CH37X)
SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)
SODIUM ACRYLATE (UNII: 7C98FKB43H)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60717-720-57	1 in 1 TUBE; Type 0: Not a Combination Product	03/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/12/2021

Labeler - RNA PHARMA, LLC (079103999)

Establishment
Name	Address	ID/FEI	Business Operations
RNA PHARMA, LLC		079103999	manufacture(60717-720)