GET MR SKINCARE DAILY PROTECTION SPF30 SUNSCREEN- zinc oxide lotion

Get Mr Skincare Daily Protection SPF30 Sunscreen by

Drug Labeling and Warnings

Get Mr Skincare Daily Protection SPF30 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Cosco International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient...........................Purpose

Zinc Oxide 18.75%..........................Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early aging caused by the sun

Warnings

• For external use only

• Do not use on damaged or borken skin

• When using this product keep out of eyes. Rinse with water to remove

• Stop use and ask a physician if rash occurs

• Keep out of reach of children.  If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally to face, neck, and ears
• use a water-resistant sunscreen if swimming or sweating
• reapply at least every two hours
• Sun Protection Measures. Spending time in the sun increases 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 10 a.m.-2 p.m.
•    wear long-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a physician 

Inactivve Ingredients

ALMOND OIL, ALPHA-TOCOPHEROL ACETATE, ASCORBIC ACID, CAPRYLYL/CAPRYL OLIGOGLUCOSIDE, CAPRYLYL GLYCOL, CETYL ALCOHOL, COCOYL CAPRYLOCAPRATE, DOCOSANOL, ETHYLHEXYLGLYCERIN, FRAGRANCE, GLYCERIN, GLYCERYL LAURATE, HEXYLENE GLYCOL, HYDROGENATED JOJOBA OIL, HYDROGENATED RAPESEED OIL, HYDROXYETHYL CELLULOSE, LACTOBIONIC ACID, MEDIUM-CHAIN TRIGLYCERIDES, NIACINAMIDE, OCTYLDODECANOL, PEG-8 DIMETHICONE, PENTYLENE GLYCOL, PHENOXYETHANOL, POLYGLYCERYL-6 DISTEARATE, POLYHYDROXYSTEARIC ACID, SAPONARIA OFFICINALIS LEAF, SILICON DIOXIDE, SODIUM CHLORIDE, SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA, VALINE, VITAMIN A PALMITATE, WATER, YELLOW WAX

Other Information

Protect this product from excessive heat and direct sun

Questions or comments?

Call toll free 1-866-438-6712

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

GET MR SKINCARE DAILY PROTECTION SPF30 SUNSCREEN 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52261-7700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	0.1875 kg  in 1 kg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERYL LAURATE (UNII: Y98611C087)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ALMOND OIL (UNII: 66YXD4DKO9)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
OCTYLDODECANOL (UNII: 461N1O614Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
YELLOW WAX (UNII: 2ZA36H0S2V)
CETYL ALCOHOL (UNII: 936JST6JCN)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROGENATED RAPESEED OIL (UNII: K168T6Y0YU)
VALINE (UNII: HG18B9YRS7)
DOCOSANOL (UNII: 9G1OE216XY)
SAPONARIA OFFICINALIS LEAF (UNII: 3988313MM7)
LACTOBIONIC ACID (UNII: 65R938S4DV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52261-7700-0	0.002 kg in 1 PACKET; Type 0: Not a Combination Product	10/01/2020
2	NDC: 52261-7700-2	1 in 1 BOX	10/01/2020
2	NDC: 52261-7700-1	0.030 kg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 52261-7700-3	0.090 kg in 1 TUBE; Type 0: Not a Combination Product	01/24/2022
4	NDC: 52261-7700-4	1 in 1 CARTON	01/25/2022
4		0.030 kg 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	10/01/2020

Labeler - Cosco International, Inc. (016433141)

Registrant - Cosco International, Inc. (016433141)

Establishment
Name	Address	ID/FEI	Business Operations
Cosco International, Inc.		016433141	manufacture(52261-7700) , label(52261-7700) , pack(52261-7700)