Label: PIPETTE MINERAL SUNSCREEN SPF 50- zinc oxide aerosol, spray
- NDC Code(s): 84723-006-01, 84723-006-02
- Packager: Pipette LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 1, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Uses
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Warnings
Warnings
. For external use only " Do not use on damaged or broken skin.
. When using this product keep out of eyes. Ainse with water to
remove. . Keep away from face to avoid breathing it. . Do not puncture or
incinerate. . Contents under pressure. . Do not store at temperatures
about 120"F .. 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.
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Directions
.Spray generously and spread evenly 15 minutes before sun exposure .
Hold container 4 to 6 inches from skin to apply. " Do not spray directly into
face. . Spray on hands then apply to face. . Do not apply in windy
conditions. . Use in well-vertilated areas. . Children under 6 months of
age: ask a doctor" reapply:" after 80 minutes of swimming or sweating"
immediately after towel drying . at least every 2 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 value of 15 or higher and take 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
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Inactive Ingredients
Water/Aqua/Eau, Caprylic/Capric Triglyceride,
Cetearyl Alcohol, Glycerin, Sorbitan Olivate, Cetyl Palmitate,
Coco-Glucoside, VP/Eicosene Copalymer, Bentonite, Polyhydroxystearic
Acid, Caprylhydroxamic Acid, Methylheptylglycerin, Polyglyceryl-3
Polyricinoleate, Isostearic Acid, Lecithin, Xanthan Gum, Squalane,
Sodium Gluconate
- Questions or comments?
- Keep out of reach of children
- Purpose
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PIPETTE MINERAL SUNSCREEN SPF 50
zinc oxide aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84723-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength SORBITAN OLIVATE (UNII: MDL271E3GR) WATER (UNII: 059QF0KO0R) COCO-GLUCOSIDE (UNII: ICS790225B) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) ISOSTEARIC ACID (UNII: X33R8U0062) XANTHAN GUM (UNII: TTV12P4NEE) GLYCERIN (UNII: PDC6A3C0OX) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) CETEARYL ALCOHOL (UNII: 2DMT128M1S) BENTONITE (UNII: A3N5ZCN45C) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) SQUALANE (UNII: GW89575KF9) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) SODIUM GLUCONATE (UNII: R6Q3791S76) CETYL PALMITATE (UNII: 5ZA2S6B08X) LECITHIN, SUNFLOWER (UNII: 834K0WOS5G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84723-006-02 1 in 1 CARTON 08/01/2025 08/01/2026 1 NDC:84723-006-01 177 mL in 1 BOTTLE, SPRAY; 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 08/01/2025 Labeler - Pipette LLC (119210873) Establishment Name Address ID/FEI Business Operations Bell International Laboratories 967781555 manufacture(84723-006)

