sunscreen lip balm

Generic: ethylhexyl methoxycinnamate, homosalate, polysilicone-15, octocrylene, butyl methoxydibenzoylmethane

Labeler: guangzhou tata biotechnology co., ltd.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sunscreen lip balm
Generic Name ethylhexyl methoxycinnamate, homosalate, polysilicone-15, octocrylene, butyl methoxydibenzoylmethane
Labeler guangzhou tata biotechnology co., ltd.
Dosage Form LIPSTICK
Routes
TOPICAL
Active Ingredients

avobenzone 2 g/100g, homosalate 6 g/100g, octinoxate 7 g/100g, octocrylene 5 g/100g, polysilicone-15 5 g/100g

Manufacturer
Guangzhou Tata Biotechnology Co., Ltd.

Identifiers & Regulatory

Product NDC 84066-101
Product ID 84066-101_4686f9b1-07a5-74cc-e063-6394a90a3afa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-01-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84066101
Hyphenated Format 84066-101

Supplemental Identifiers

UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 5A68WGF6WM F8DRP5BB29

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 lip balm (source: ndc)
Generic Name ethylhexyl methoxycinnamate, homosalate, polysilicone-15, octocrylene, butyl methoxydibenzoylmethane (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2 g/100g
  • 6 g/100g
  • 7 g/100g
  • 5 g/100g
source: ndc
Packaging
  • 3.2 g in 1 TUBE (84066-101-01)
source: ndc

Packages (1)

84066-101-01 3.2 g in 1 TUBE (84066-101-01)

Ingredients (5)

avobenzone (2 g/100g) homosalate (6 g/100g) octinoxate (7 g/100g) octocrylene (5 g/100g) polysilicone-15 (5 g/100g)

Linked Drug Pages (1)

SUNSCREEN LIP BALM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4686f9b1-07a5-74cc-e063-6394a90a3afa", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "5A68WGF6WM", "F8DRP5BB29"], "spl_set_id": ["0f8e08bf-4b14-bdad-e063-6394a90a34e1"], "manufacturer_name": ["Guangzhou Tata Biotechnology Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3.2 g in 1 TUBE (84066-101-01)", "package_ndc": "84066-101-01", "marketing_start_date": "20240125"}], "brand_name": "SUNSCREEN LIP BALM", "product_id": "84066-101_4686f9b1-07a5-74cc-e063-6394a90a3afa", "dosage_form": "LIPSTICK", "product_ndc": "84066-101", "generic_name": "Ethylhexyl Methoxycinnamate, Homosalate, Polysilicone-15, Octocrylene, Butyl Methoxydibenzoylmethane", "labeler_name": "Guangzhou Tata Biotechnology Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNSCREEN LIP BALM", "active_ingredients": [{"name": "AVOBENZONE", "strength": "2 g/100g"}, {"name": "HOMOSALATE", "strength": "6 g/100g"}, {"name": "OCTINOXATE", "strength": "7 g/100g"}, {"name": "OCTOCRYLENE", "strength": "5 g/100g"}, {"name": "POLYSILICONE-15", "strength": "5 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240125", "listing_expiration_date": "20261231"}