EQUALINE ZINC OXIDE SUNSCREEN STICK SPF 50- zinc oxide stick

Equaline Zinc Oxide Sunscreen Stick SPF 50 by

Drug Labeling and Warnings

Equaline Zinc Oxide Sunscreen Stick SPF 50 by is a Otc medication manufactured, distributed, or labeled by United Natural Foods, Inc. dba UNFI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 21.6%

Purpose

Sunscreen

Uses

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

Warnings

For external use only

Do not use

on damaged or broken skin.

When using this product 

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs.

Keep out of reach of children.

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

Directions

• apply liberally 15 minutes before sun exposure
• reapply:

after 80 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

• children under 6 months of age: Ask a doctor
• 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 value 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-sleeved shirts, pants, hats, and sunglasses

Other Information

• protect the product in this container from excessive heat and direct sun
• may stain or damage some fabrics, materials or surfaces

Inactive Ingredient(s)

beeswax, butyloctyl salicylate, caprylyl/ capric triglyceride, caprylyl glycol, cetyl alcohol, euphorbia cerifera (candelilla) wax, fragrance, isopropyl palmitate, isostearic acid, neopentyl glycol diethylhexanoate, ozokerite, polyhydroxystearic acid, silica

Label

INGREDIENTS AND APPEARANCE

EQUALINE ZINC OXIDE SUNSCREEN STICK SPF 50 
zinc oxide stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-969
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
CANDELILLA WAX (UNII: WL0328HX19)
SUNFLOWER OIL (UNII: 3W1JG795YI)
WHITE WAX (UNII: 7G1J5DA97F)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
ISOSTEARIC ACID (UNII: X33R8U0062)
CETYL ALCOHOL (UNII: 936JST6JCN)
COCOA BUTTER (UNII: 512OYT1CRR)
CERESIN (UNII: Q1LS2UJO3A)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41163-969-28	42 g in 1 CONTAINER; Type 0: Not a Combination Product	09/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/14/2023

Labeler - United Natural Foods, Inc. dba UNFI (943556183)