NORWEX LIP GLAZE BROAD SPECTRUM SPF 30 HAZELNUT- zinc oxide lipstick

Norwex Lip Glaze Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Norwex Lip Glaze Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by Norwex Usa, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Zinc Oxide 13.9%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only

Do not use

on damaged of 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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply generously 15 minutes before sun exposure
• Children under 6 months of age:ask a doctor.
• reapply at least every 2 hours
• use a water-resistant sunscreen if swimming or sweating
• ​Sun Protection Measures ​Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularyly use a sunscreen with a Broad Spectrum value of SPF 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 shiirts, pants, hats and sunglasses

Other Information

Protect the product in this container from excessive heat and direct sun

Inactive ingredients

Diisostearyl malate, polybutene, hydrogenated polyisobutene, butyloctyl salicylate, microcrystalline wax/cire microcristalline, silica dimethyl silylate, caprylic/capric triglyceride, bis-diglyceryl polyacyladipate-2, sorbitan olivate, isononyl isononanoate, polyhydroxystearic acid, sorbitan isostearate, isostearic acid, lecithin, polyglyceryl-3 polyricinoleate, VP/hexadecene copolymer, flavor/aroma, menthone glycerin acetal, dehydroacetic acid, tocopherol, iron oxides/CI 77491, CI 77499

Questions?

Call 1-866-450-7499

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NORWEX LIP GLAZE BROAD SPECTRUM SPF 30  HAZELNUT
zinc oxide lipstick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80971-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	139 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
ISOSTEARIC ACID (UNII: X33R8U0062)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
MENTHONE GLYCERIN ACETAL (UNII: 7QQ1EE6RCP)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80971-103-02	1 in 1 CARTON	12/01/2025
1	NDC: 80971-103-01	17 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 Drug	M020	12/01/2025

Labeler - Norwex Usa, Inc. (016707931)