Label: BELIF THE TRUE CREAM AQUA BOMB SUNSCREEN BROAD SPECTRUM SPF 45- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 53208-721-50
- Packager: LG H&H Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 19, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DIRECTIONS
- Apply generously 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. - 2 p.m.
- Wear long-sleeved shirts, pants, hats, and sunglasses.
- Children under 6 months: Ask a doctor.
- INACTIVE INGREDIENTS
- OTHER INFORMATION
- QUESTIONS OR COMMENTS?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL
belif
believe in truthThe true cream -
aqua bomb sunscreen
Broad Spectrum SPF 45
Lightweight moisturizer and sun protection
in one? Yes!Hydrates skin with lightweight texture
------------------------------------------------------------ YesNo visible white cast
------------------------------------------------------------ YesOur belief to deliver explosive hydration and
UVA/UVB protection to your skin. This
moisturizing sunscreeen keeps your skin's
moisture barrier replenished, provides SPF 45,
and leaves no white cast or greasiness after
application. Also, this product is formulated
with a washable formula to provide easy
removal when washing the face with a cleanser.(PROTECTION UVA/UVB)
(NIACINAMIDE)
(NO VISIBLE WHITE CAST)
(FOR ALL SKIN TYPES)
Dermatologically tested
50 ml / 1.69 fl. oz.
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INGREDIENTS AND APPEARANCE
BELIF THE TRUE CREAM AQUA BOMB SUNSCREEN BROAD SPECTRUM SPF 45
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-721 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 50 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 50 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.7 g in 50 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53208-721-50 1 in 1 BOX 02/29/2024 1 50 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 02/29/2024 Labeler - LG H&H Co.,Ltd. (688276187) Establishment Name Address ID/FEI Business Operations fmg Co.Ltd 690188305 manufacture(53208-721)