FDA.reportPublic FDA data

Doc Block Daily Sunscreen Broad Spectrum SPF55

Product NDC
71873-101
11-digit product format
718730101
Labeler code
71873
Product ID
71873-101_72df9f91-0c2e-4b88-e053-2991aa0af81b
Type
HUMAN OTC DRUG
Nonproprietary name
sunscreen
Dosage form
LOTION
Route
TOPICAL
Labeler
Garth Fisher Beauty LLC
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-06-08
Marketing end
0000-00-00
Substance
OCTOCRYLENE; HOMOSALATE; AVOBENZONE; OCTISALATE
Active strength
7 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71873-101-112021-02-18C16284748780-19d75b9d0-0ad5-f424-e053-dadaa90a57ce72ca6413-402f-1626-e053-2991aa0a73ae
71873-101-122021-02-18C16284748780-19d75b9d0-0ad5-f424-e053-dadaa90a57ce72ca6413-402f-1626-e053-2991aa0a73ae
71873-101-112020-01-31C16284748780-19d75b9d0-0ad5-f424-e053-dadaa90a57ce72ca6413-402f-1626-e053-2991aa0a73ae
71873-101-122020-01-31C16284748780-19d75b9d0-0ad5-f424-e053-dadaa90a57ce72ca6413-402f-1626-e053-2991aa0a73ae