FIRST AID BEAUTY FAB ULTRA LIGHT MINERAL SUNSCREEN BROAD SPECTRUM SPF 30- zinc oxide liquid

First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Zinc oxide 22%

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

Directions

• shake well before use
• apply liberally 15 minutes before sun exposure
• reapply at least every 2 hours
• use 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, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in sun, especially from 10 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months: ask a doctor

Other information

• protect this product from excessive heat and direct sun

Inactive ingredients

Ethylhexyl olivate, isododecane, coconut alkanes, water, aluminum starch octenylsuccinate, caprylic/capric triglyceride, butylene glycol, mica, polyglyceryl-6 polyricinoleate, jojoba esters, cellulose, stearalkonium hectorite, sodium chloride, squalane, polyglyceryl-3 diisostearate, polyglyceryl-3 polyricinoleate, iron oxides, phenoxyethanol, tocopheryl acetate, coco-caprylate/caprate, trihydroxystearin, caprylyl glycol, polyhydroxystearic acid, glycerin, trisodium ethylenediamine disuccinate, propanediol, sorbic acid, titanium dioxide, silica, glycyrrhiza glabra (licorice) root extract, camellia sinensis leaf extract, alumina, tocopherol, chrysanthemum parthenium (feverfew) extract

Questions?

888-FAB-3063

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MADE IN USA.

FIRST AID BEAUTY ® LTD
NEWTON, MA 02458.

WWW.FIRSTAIDBEAUTY.COM

PRINCIPAL DISPLAY PANEL

FIRST AID BEAUTY ​®

FAB

Ultra Light

Mineral

Sunsceren

with Zinc Oxide

Broad Spectrum SPF 30

1.5 FL OZ (44 mL)

INGREDIENTS AND APPEARANCE

FIRST AID BEAUTY FAB ULTRA LIGHT MINERAL SUNSCREEN BROAD SPECTRUM SPF 30 
zinc oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-214
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	22 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYL OLIVATE (UNII: HTC7G3S2PV)
FERROUS OXIDE (UNII: G7036X8B5H)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)
POLYGLYCERYL-10 POLYRICINOLEATE (UNII: DHM1T5XO11)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
GLYCYRRHIZA GLABRA (LICORICE) ROOT (UNII: 2788Z9758H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ALUMINA (UNII: LMI26O6933)
MICA (UNII: V8A1AW0880)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
COCONUT ALKANES (UNII: 1E5KJY107T)
ISODODECANE (UNII: A8289P68Y2)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
SILICA (UNII: ETJ7Z6XBU4)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SQUALANE (UNII: GW89575KF9)
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
PROPANEDIOL (UNII: 5965N8W85T)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SORBIC ACID (UNII: X045WJ989B)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-214-44	1 in 1 CARTON	07/01/2025
1		44 mL in 1 BOTTLE, PLASTIC; 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	07/01/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)