h.e.b ultra

Generic: spf 50 sunscreen

Labeler: h.e.b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name h.e.b ultra
Generic Name spf 50 sunscreen
Labeler h.e.b
Dosage Form AEROSOL, SPRAY
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 100 mg/mL, octisalate 45 mg/mL, octocrylene 80 mg/mL

Manufacturer
H.E.B

Identifiers & Regulatory

Product NDC 37808-914
Product ID 37808-914_c6b84cf6-4361-5352-e053-2995a90a2717
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2019-02-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808914
Hyphenated Format 37808-914

Supplemental Identifiers

UPC
0041220721702
UNII
G63QQF2NOX V06SV4M95S 4X49Y0596W 5A68WGF6WM

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 h.e.b ultra (source: ndc)
Generic Name spf 50 sunscreen (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 100 mg/mL
  • 45 mg/mL
  • 80 mg/mL
source: ndc
Packaging
  • 237 mL in 1 TUBE (37808-914-12)
source: ndc

Packages (1)

37808-914-12 237 mL in 1 TUBE (37808-914-12)

Ingredients (4)

avobenzone (30 mg/mL) homosalate (100 mg/mL) octisalate (45 mg/mL) octocrylene (80 mg/mL)

Linked Drug Pages (1)

H.E.B ULTRA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "c6b84cf6-4361-5352-e053-2995a90a2717", "openfda": {"upc": ["0041220721702"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["d6184ba2-0e47-459a-8777-1f27be2140a6"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 TUBE (37808-914-12)", "package_ndc": "37808-914-12", "marketing_start_date": "20190205"}], "brand_name": "H.E.B ULTRA", "product_id": "37808-914_c6b84cf6-4361-5352-e053-2995a90a2717", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "37808-914", "generic_name": "SPF 50 Sunscreen", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B ULTRA", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190205", "listing_expiration_date": "20261231"}