HERBALIFE SKIN PROTECTIVE MOISTURIZER BROAD SPECTRUM SPF 30 MINERAL SUNSCREEN- zinc oxide cream

Herbalife SKIN Protective Moisturizer Broad Spectrum SPF 30 Mineral Sunscreen by

Drug Labeling and Warnings

Herbalife SKIN Protective Moisturizer Broad Spectrum SPF 30 Mineral Sunscreen by is a Otc medication manufactured, distributed, or labeled by Herbalife International of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

PURPOSE

Purpose

Sunscreen

ACTIVE INGREDIENT

Active ingredient

Zinc Oxide (17.5%)

INDICATIONS & USAGE

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

Warnings
For external use only

DO NOT USE

Do not use on damaged or broken
skin

WHEN USING

When using this product 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
swallowed, get medical help or contact
a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
Apply liberally 15 minutes before sun
exposure
Reapply at least every 2 hours
Use a water resistant sunscreen if
swimming or sweating
Children under 6 months: 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

STORAGE AND HANDLING

Other information

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

INACTIVE INGREDIENT

Inactive ingredients:

Water (Aqua), Caprylic/Capric
Triglyceride, Glycerin, Cetearyl Alcohol,
Coco-Glucoside, Silica, Aloe Barbadensis
Leaf Juice, Niacinamide, Tetrahexyldecyl
Ascorbate, Tocopheryl Acetate, Physalis
Angulata Extract, Cocoyl Proline,
Lecithin, Isostearic Acid, Polyglyceryl-3
Polyricinoleate, Polyhydroxystearic Acid,
Xanthan Gum, Fragrance (Parfum),
Disodium EDTA, Ethylhexylglycerin,
Hexylene Glycol, Caprylyl Glycol,
Phenoxyethanol.

SPL UNCLASSIFIED SECTION

Distributed by:
Herbalife International of America, Inc.
800 W. Olympic Blvd., Suite 406,
Los Angeles, CA 90015, USA
Made in USA with US
and imported ingredients.

CUT0899NA0A-00
©2021 HERBALIFE NUTRITION

PRINCIPAL DISPLAY PANEL

HERBALIFE

SKIN

5

Protective Moisturizer
Broad Spectrum SPF 30
Mineral Sunscreen

Sunscreen cream

1 fl oz (30 ml)

INGREDIENTS AND APPEARANCE

HERBALIFE SKIN PROTECTIVE MOISTURIZER BROAD SPECTRUM SPF 30 MINERAL SUNSCREEN 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51785-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	17.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
COCO GLUCOSIDE (UNII: ICS790225B)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ISOSTEARIC ACID (UNII: X33R8U0062)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHYSALIS ANGULATA (UNII: W4TKW9D5GG)
NIACINAMIDE (UNII: 25X51I8RD4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
COCOYL PROLINE (UNII: 0IH06971TF)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51785-900-00	1 in 1 CARTON	05/01/2022
1		30 mL in 1 BOTTLE, PUMP; 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	05/01/2022

Labeler - Herbalife International of America Inc. (873035968)