Label: SHEER GLOW- zinc oxide cream
- NDC Code(s): 70809-1910-1, 70809-1910-2
- Packager: USRX LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Purpose
- Use(s):
- Warnings:
-
Directions:
For Sunscreen use:
- Apply liberally and evenly 15 minutes before sun exposure
- 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, 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. to 2 p.m.
- Wear long-sleeved shirts, pants, hats and sunglasses
- Children under 6 months: ask a doctor
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INACTIVE INGREDIENTS:
Water (Aqua), Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Glycerin, Dimethicone, Undecylcrylene Dimethicone, Cetearyl Olivate, Polyester-8, Polyglyceryl-3 Beeswax, Carthamus Tinctorius (Safflower) Oleosomes, Sorbitan Olivate, Propanediol, Polyhydroxystearic Acid, Potassium Cetyl Phosphate, Caprylyl Glycol, Hydrolyzed Wheat Protein/PVP Crosspolymer, Xanthan Gum, Bisabolol, Caprylhydroxamic Acid, Sodium Gluconate, Citrus Reticulata (Tangerine) Peel Oil, Carthamus Tinctorius (Safflower) Seedcake Extract, Citrus Grandis (Grapefruit) Fruit Extract.
- Other Information:
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SHEER GLOW
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70809-1910 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 11.6 mg in 100 mL Inactive Ingredients Ingredient Name Strength PUMMELO (UNII: ET1TN5W71X) MANDARIN OIL (UNII: NJO720F72R) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) PROPANEDIOL (UNII: 5965N8W85T) XANTHAN GUM (UNII: TTV12P4NEE) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) LEVOMENOL (UNII: 24WE03BX2T) SODIUM GLUCONATE (UNII: R6Q3791S76) UNDECYLCRYLENE DIMETHICONE (10000 MW) (UNII: HA26P2LA4P) WATER (UNII: 059QF0KO0R) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70809-1910-1 1 in 1 BOX 07/19/2001 1 66.5 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:70809-1910-2 1 in 1 BOX 06/01/2021 2 15 mL 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 07/19/2001 Labeler - USRX LLC (115270633)
