SELF REFLECT PROBIOTIC SUNSCREEN MOISTURIZER BROAD SPECTRUM SPF 32- zinc oxide cream

Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum SPF 32 by

Drug Labeling and Warnings

Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum SPF 32 by is a Otc medication manufactured, distributed, or labeled by Allure Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Zinc Oxide 22.4%

PURPOSE

Purpose: Sunscreen

INDICATIONS & USAGE

Uses:

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Direction), decreases the risk of skin cancer and  early skin aging caused by the sun.

WARNINGS AND PRECAUTIONS

Warning: For external use only.

DO NOT USE

Do not use: on damaged or broken skin.

WHEN USING

When using this products:

• Keep out of eyes.
• Rinse with water to remove.
  

STOP USE

Stop use and ask a doctor: If rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

• If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• Apply generously 15 minutes before sun exposer.
• Use a water resistant sunscreen if swimming or sweating. 
• Reapply at least every 2 hours.
• Sun protection measures: Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10am - 2pm.
• Wear long sleeved shirts, pants, hats and sunglasses.
• Children under 6 months: Ask a doctor.

Other Information: Protect the product from excessive heat and direct sun.

INACTIVE INGREDIENT

Inactive Ingredients: Water (Aqua), Caprylyc/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Pyrus Malus (Apple) Fruit Extract, Coco-Glucoside, Lactobacillus Ferment, Rubus Idaeus (Red Rasberry) Seed Oil, Cocos Nucifera (Coconut) Liquid Endosperm, Curcuma Longa (Turmeric) Rhizomes Oil, Butyrospermum Parkii Nut Extract, Hydrolyzed Jojoba Esters, Tocopherol, Dipotassium Glycyrrhizate, Vanilla Planifolia Fruit Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Butylene Glycol, Isostearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Polyhydroxystearic Acid, Coco-Caprylate/Caprate, Caprylyl/Capryl Glucoside, Sclerotium Gum, Cetearyl Glucoside, Ethylhexylglycerin, Xanthan Gum, Octyldodecanol, Tapioca Starch, Citric Acid, Sorbitan Oleate, Phenoxyethanol, Sodium Benzoate, Potassium Sorbate, May contains +/- Iron Oxides (Cl77491, Cl77492)

QUESTIONS

Questions or Comments?

Call toll free (877) 456-2582

PRINCIPAL DISPLAY PANEL

Kinship Inc.,

Corte Modera, CA 94925

Made in USA

lovekinship.com

INGREDIENTS AND APPEARANCE

SELF REFLECT PROBIOTIC SUNSCREEN MOISTURIZER BROAD SPECTRUM SPF 32 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4181
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	224 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
COCONUT ALKANES (UNII: 1E5KJY107T)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
APPLE (UNII: B423VGH5S9)
COCO GLUCOSIDE (UNII: ICS790225B)
LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
RASPBERRY SEED OIL (UNII: 9S8867952A)
COCONUT WATER (UNII: 267F5Y81NT)
TURMERIC OIL (UNII: 6KGS8SP16U)
SHEANUT (UNII: 84H6HBP32L)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
VANILLA (UNII: Q74T35078H)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ISOSTEARIC ACID (UNII: X33R8U0062)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
XANTHAN GUM (UNII: TTV12P4NEE)
OCTYLDODECANOL (UNII: 461N1O614Y)
STARCH, TAPIOCA (UNII: 24SC3U704I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4181-2	1 in 1 CARTON	12/12/2019
1	NDC: 62742-4181-1	50 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	12/12/2019

Labeler - Allure Labs Inc (926831603)