ea eight hour skin protectant
Generic: petrolatum
Labeler: revlonDrug Facts
Product Profile
Brand Name
ea eight hour skin protectant
Generic Name
petrolatum
Labeler
revlon
Dosage Form
EMULSION
Routes
Active Ingredients
petrolatum 56.8 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
10967-672
Product ID
10967-672_3b516086-ba84-c160-e063-6294a90a78af
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2016-02-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10967672
Hyphenated Format
10967-672
Supplemental Identifiers
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
ea eight hour skin protectant (source: ndc)
Generic Name
petrolatum (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 56.8 mg/g
Packaging
- 50 g in 1 TUBE (10967-672-17)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3b516086-ba84-c160-e063-6294a90a78af", "openfda": {"unii": ["4T6H12BN9U"], "spl_set_id": ["b590991c-8ec8-67c2-e053-2a95a90a3acf"], "manufacturer_name": ["REVLON"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (10967-672-17)", "package_ndc": "10967-672-17", "marketing_start_date": "20160216"}], "brand_name": "EA EIGHT HOUR SKIN PROTECTANT", "product_id": "10967-672_3b516086-ba84-c160-e063-6294a90a78af", "dosage_form": "EMULSION", "product_ndc": "10967-672", "generic_name": "PETROLATUM", "labeler_name": "REVLON", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EA EIGHT HOUR SKIN PROTECTANT", "active_ingredients": [{"name": "PETROLATUM", "strength": "56.8 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160216", "listing_expiration_date": "20261231"}