h.e.b solutions sunscreen

Generic: ultra spf 50 lotion

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

Drug Facts

Product Profile

Brand Name h.e.b solutions sunscreen
Generic Name ultra spf 50 lotion
Labeler h.e.b
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 20 mg/mL, homosalate 100 mg/mL, octisalate 50 mg/mL, octocrylene 70 mg/mL, oxybenzone 60 mg/mL

Manufacturer
H.E.B

Identifiers & Regulatory

Product NDC 37808-956
Product ID 37808-956_248a0777-7394-dea1-e063-6394a90a444a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2012-02-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808956
Hyphenated Format 37808-956

Supplemental Identifiers

UPC
0041220898954 0041220898930
UNII
G63QQF2NOX V06SV4M95S 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 h.e.b solutions sunscreen (source: ndc)
Generic Name ultra spf 50 lotion (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
  • 100 mg/mL
  • 50 mg/mL
  • 70 mg/mL
  • 60 mg/mL
source: ndc
Packaging
  • 89 mL in 1 TUBE (37808-956-09)
  • 237 mL in 1 TUBE (37808-956-12)
source: ndc

Packages (2)

37808-956-09 89 mL in 1 TUBE (37808-956-09) 37808-956-12 237 mL in 1 TUBE (37808-956-12)

Ingredients (5)

avobenzone (20 mg/mL) homosalate (100 mg/mL) octisalate (50 mg/mL) octocrylene (70 mg/mL) oxybenzone (60 mg/mL)

Linked Drug Pages (1)

H.E.B Solutions Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "248a0777-7394-dea1-e063-6394a90a444a", "openfda": {"upc": ["0041220898954", "0041220898930"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["12c76c72-4411-48d5-b79b-c58703bf1fdd"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 TUBE (37808-956-09)", "package_ndc": "37808-956-09", "marketing_start_date": "20120220"}, {"sample": false, "description": "237 mL in 1 TUBE (37808-956-12)", "package_ndc": "37808-956-12", "marketing_start_date": "20120220"}], "brand_name": "H.E.B Solutions Sunscreen", "product_id": "37808-956_248a0777-7394-dea1-e063-6394a90a444a", "dosage_form": "LOTION", "product_ndc": "37808-956", "generic_name": "Ultra SPF 50 Lotion", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B", "brand_name_suffix": "Solutions Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "20 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "70 mg/mL"}, {"name": "OXYBENZONE", "strength": "60 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120220", "listing_expiration_date": "20261231"}