h.e.b baby
Generic: spf 50 sunscreen
Labeler: h.e.bDrug Facts
Product Profile
Brand Name
h.e.b baby
Generic Name
spf 50 sunscreen
Labeler
h.e.b
Dosage Form
AEROSOL, SPRAY
Routes
Active Ingredients
avobenzone 30 mg/mL, homosalate 100 mg/mL, octisalate 45 mg/mL, octocrylene 80 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-913
Product ID
37808-913_2489deb6-247b-7026-e063-6394a90ab5eb
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
37808913
Hyphenated Format
37808-913
Supplemental Identifiers
UPC
UNII
Packaging Origin
Original Packager
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 baby (source: ndc)
Generic Name
spf 50 sunscreen (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
- 100 mg/mL
- 45 mg/mL
- 80 mg/mL
Packaging
- 237 mL in 1 TUBE (37808-913-12)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2489deb6-247b-7026-e063-6394a90ab5eb", "openfda": {"upc": ["0041220721771"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["61273611-ab7a-4216-aebe-2c8d89660281"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 TUBE (37808-913-12)", "package_ndc": "37808-913-12", "marketing_start_date": "20190205"}], "brand_name": "H.E.B BABY", "product_id": "37808-913_2489deb6-247b-7026-e063-6394a90ab5eb", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "37808-913", "generic_name": "SPF 50 Sunscreen", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B BABY", "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"}