sunscreen moisturizer spf 30

Generic: avobenzone octinoxate octisalate oxybenzone homosalate octocrylene

Labeler: skin authority llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sunscreen moisturizer spf 30
Generic Name avobenzone octinoxate octisalate oxybenzone homosalate octocrylene
Labeler skin authority llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 3 g/100mL, homosalate 7 g/100mL, octinoxate 7.5 g/100mL, octisalate 5 g/100mL, octocrylene 3 g/100mL, oxybenzone 6 g/100mL

Manufacturer
Skin Authority LLC

Identifiers & Regulatory

Product NDC 46007-203
Product ID 46007-203_4642868b-77c1-411e-e063-6394a90ac676
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2012-04-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46007203
Hyphenated Format 46007-203

Supplemental Identifiers

UPC
0853926003750 0853926003156
UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 4X49Y0596W 5A68WGF6WM 95OOS7VE0Y

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sunscreen moisturizer spf 30 (source: ndc)
Generic Name avobenzone octinoxate octisalate oxybenzone homosalate octocrylene (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3 g/100mL
  • 7 g/100mL
  • 7.5 g/100mL
  • 5 g/100mL
  • 6 g/100mL
source: ndc
Packaging
  • 20 mL in 1 TUBE (46007-203-21)
  • 118 mL in 1 TUBE (46007-203-24)
source: ndc

Packages (2)

46007-203-21 20 mL in 1 TUBE (46007-203-21) 46007-203-24 118 mL in 1 TUBE (46007-203-24)

Ingredients (6)

avobenzone (3 g/100mL) homosalate (7 g/100mL) octinoxate (7.5 g/100mL) octisalate (5 g/100mL) octocrylene (3 g/100mL) oxybenzone (6 g/100mL)

Linked Drug Pages (1)

SUNSCREEN MOISTURIZER SPF 30 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4642868b-77c1-411e-e063-6394a90ac676", "openfda": {"upc": ["0853926003750", "0853926003156"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["522ed1ed-4935-4b7c-a21a-ebd697a9a749"], "manufacturer_name": ["Skin Authority LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 TUBE (46007-203-21)", "package_ndc": "46007-203-21", "marketing_start_date": "20120419"}, {"sample": false, "description": "118 mL in 1 TUBE (46007-203-24)", "package_ndc": "46007-203-24", "marketing_start_date": "20120419"}], "brand_name": "SUNSCREEN MOISTURIZER SPF 30", "product_id": "46007-203_4642868b-77c1-411e-e063-6394a90ac676", "dosage_form": "LOTION", "product_ndc": "46007-203", "generic_name": "AVOBENZONE OCTINOXATE OCTISALATE OXYBENZONE HOMOSALATE OCTOCRYLENE", "labeler_name": "Skin Authority LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNSCREEN MOISTURIZER", "brand_name_suffix": "SPF 30", "active_ingredients": [{"name": "AVOBENZONE", "strength": "3 g/100mL"}, {"name": "HOMOSALATE", "strength": "7 g/100mL"}, {"name": "OCTINOXATE", "strength": "7.5 g/100mL"}, {"name": "OCTISALATE", "strength": "5 g/100mL"}, {"name": "OCTOCRYLENE", "strength": "3 g/100mL"}, {"name": "OXYBENZONE", "strength": "6 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120419", "listing_expiration_date": "20261231"}